Tag | Content |
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EnhancerAtlas ID | HS134-00341 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:16465500-16469190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr1:16466266-16466277 | AAGCAATAAAA | + | 6.32 | RREB1 | MA0073.1 | chr1:16467768-16467788 | CCAGGGGGGTTGGTTGGGGT | - | 6.93 | ZNF263 | MA0528.1 | chr1:16468206-16468227 | AGAGGAGGAAGTGGGGGAAGA | + | 7.89 |
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| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_01311 | chr1:16465054-16467084 | Adrenal_Gland | SE_01311 | chr1:16467161-16468607 | Adrenal_Gland | SE_23091 | chr1:16465053-16466236 | Colon_Crypt_1 | SE_23091 | chr1:16466252-16467025 | Colon_Crypt_1 | SE_23751 | chr1:16465457-16465897 | Colon_Crypt_2 | SE_24743 | chr1:16465421-16465897 | Colon_Crypt_3 | SE_26540 | chr1:16464423-16467134 | Esophagus | SE_26540 | chr1:16467219-16474484 | Esophagus | SE_29455 | chr1:16467791-16468550 | Fetal_Intestine_Large | SE_30715 | chr1:16467395-16468971 | Fetal_Muscle | SE_31527 | chr1:16465065-16467061 | Gastric | SE_31527 | chr1:16467241-16474177 | Gastric | SE_34268 | chr1:16463915-16469522 | HCT-116 | SE_34628 | chr1:16464389-16475128 | HeLa | SE_36144 | chr1:16465332-16467155 | HMEC | SE_36144 | chr1:16467369-16469082 | HMEC | SE_38062 | chr1:16464574-16469506 | HUVEC | SE_40833 | chr1:16464800-16474529 | Left_Ventricle | SE_42443 | chr1:16464217-16474534 | Lung | SE_44998 | chr1:16465283-16466252 | NHLF | SE_44998 | chr1:16466301-16467125 | NHLF | SE_44998 | chr1:16467852-16468802 | NHLF | SE_46140 | chr1:16464962-16469237 | Osteoblasts | SE_47150 | chr1:16463762-16486412 | Panc1 | SE_48744 | chr1:16464918-16474528 | Right_Atrium | SE_52536 | chr1:16464905-16467041 | Small_Intestine | SE_52536 | chr1:16467684-16469210 | Small_Intestine | SE_53900 | chr1:16464743-16469386 | Spleen | SE_56795 | chr1:16467226-16474542 | VACO_400 | SE_64726 | chr1:16467542-16468812 | NHEK | SE_65472 | chr1:16465146-16466178 | Pancreatic_islets | SE_65472 | chr1:16466192-16467043 | Pancreatic_islets | SE_65472 | chr1:16467559-16468683 | Pancreatic_islets | SE_69141 | chr1:16464511-16467047 | H9 | SE_69141 | chr1:16467939-16468895 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I016137 | chr1 | 16464252 | 16469121 |
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Enhancer Sequence | CTGACCAGGA AGCAGGAAAG GCCAAGCCCC CTGGCATTTT CTCTGGCTCT GCTTCCAGGA 60 CCGAGTCATA TCCGCCACTC ACAAGGACAG CCAGGAAGTG ACTCTTCCTC CCCCAGTGGC 120 CAGTCCTGTC CTGGCCCAGC AGGCTGGGGG CTCAGGCACC TGACTCCGGG GGCTTCTTCC 180 TCCCACCGCC CTATCCTGTC TCATCCCGCC CCTGCCCTAA GCCCCTTCCT GGCCCTACAG 240 GCAGGAAGCT GCCCAGACAC AGGGCTCACG GTGCAGGGCT GTCCAGGGCT TGGGCAGCTG 300 CTGAAGTGGC CAGGGTGGGT AGAGGTCACC CTAGGGAGCT CCTCCAACAA CCCTACAATT 360 ATAATCCTTC AGATTGTTCT GATGAGAGGG TCCTGAGACA CCTCCAACCT CAGCACCGTG 420 TTCACCACAC ACACAATGAT CCTCTGCTCT GTGCCTGGCC CACCCCCAGT GCTGGGTATG 480 CACCAAGATG AAAACAAACT CCTGATCTCA GGGAGCAGAA GCACCTGACA AGGTCTGCAA 540 GACAGAGGGA GGAAACAAGC TAACAGCTAA GGGGGTGGAG AAGGGGAAAC AACCTTGGCC 600 AGGAGTCTGA GAAGTCACAG AGGGGACATT TTGGCTGGGG TTCAGAGGCT GCATAGGAGT 660 TCAGCAGGGG AATGATAGAT GTTGGGAGAG GGAGTTAGGA GTGAGAAAGT GCATGACTAA 720 TACGGAAGGT ATGAGTGGGT TTGTGGGCAC AAATGTGGGG AGCAGCAAGC AATAAAACAG 780 TTGAGAAAGG CCTTCAATGC CAGGCCAAGA AGCTGGGACT TTATCCTGGA GGCAATGGAA 840 AGCCGCTGGA GGTCTGATGT GGAGAAGTCA GACCCCTGCC GTCAGGAAAA ATCTGTGCCT 900 GGAGGCAGCT TTTGTCCAAG ACCCTGGGGA CAACCTGGCC CCTAATGGCC TAAGGACAAC 960 CCCCTCCAGG GAAGCAATTT CAAGTGCCCT GACCCAAGCA AACCTGCTAA CTCTCAGGGA 1020 CAGAATCTGG AGCGAAGACT CTCGTCATCC AGTCCCCTGT GTGAGCAGAG GTGCAGAGGG 1080 GGACCAGGAG TCAGGGGAAC AGGACTCAAA GGACACCCAG CTCTGTAAGG TGCCAGATAG 1140 TGACCTCCTG CTGATGACTC TGCTCTCAGA GCCAGGCTGC ATCCCTGTCC CCTCCCAACC 1200 CTGGCCCAGG GACCACACAA ACAGCCGCTC TCACCCCCTT GGTCCATCCT GCTTCTGCAG 1260 ACCCTCAGCA TTGGCCCTGC AAGAGCTCAG GCACATAGGG CAGGGAAGGG GGCTTGTCCC 1320 AGGTCATGCA GCAGGACAGA GGAGGCCCGG GACCCGACTC CTGCTCTGCA CAGAGCCTGG 1380 AGTCCCAATG ACAGTACCTA CTATGCGCAG GGCTCGGGCT AAGCACTGTA CCCTCATTTA 1440 GTCCTCGCAA TAGACCTGCT ATATACAGGC ACTATTAGCG CTGGTTCCAC TTTGGAGGTG 1500 AGGAGAGACA AAAAAGCTTG TCCAAGGTCA CCAAGCTCCC AAGAAGGAAA CCAGAACTCA 1560 AACTTAGGAT GCCTGATTTT CAGCCTCTCT CCTCTCCCAC TCCTTTTTCA TTATTTATTT 1620 ATTTTGTTTT TGAGATGGAG TCTCGCTCTG TTGCCCAGGC TGGAGTGAAG TGGTGGGATC 1680 TCAGCTCACT GCAACCTCCG CCTCCTGGGT TCAAGCAATT CTCCTGCCTC AGCCTCCTGA 1740 GTAGCTGGAA CTACAGGCAC CGGCCATCAA GCCTGGCTAA CTTTTGTATT TTTAGTAGAG 1800 ATGCAGCCTG GTCTCGAACT CCTGGCCTCA AGTGATCCAC CCGTCTCGGC CTCCCAAAGT 1860 GCTGGGATTA CAGGCGTGAG CCACCGCGTC CGGCCTATTT TATTTTTTAG AGACGGGGTG 1920 TGTCTTTGTT GCCCAGGCTG GTCTCTTGAC CTCCTGGCCT CAAGTGATCC TCCCACCTCG 1980 ACTTCCCACA ATGCTGGGAT TACAGGCGTG AGCCACCTCA CCGGGCCTCC TTTCCCACTT 2040 CTGTTCTTAG GAACACTTCA ATTTGGAGCA AAGATAAATC AACATTCTGA AACAAGCCTG 2100 AAGAGAGAGG AGATAAGGCC TGACCCACTT CAAAAGCCAG AAACTCCTGA CGAATTTCAG 2160 AGCAGCTGTG GGTCTATGTG TTGTGGAGGA GGGGAGGGTA TTCCCCACCA CAGATCTTCT 2220 CAAACTGGGC ACTTTTGTGT CTGTGAGCAG AAAAGTGTAG ACTCCAGCCC AGGGGGGTTG 2280 GTTGGGGTGG CTGAAGTGGT CTCCTTCAAG CCCCGAATGT CTTCAAGTCT CCTATTGTAT 2340 TTGGAAACCC ATGAGTATAT TGCATCCCTC CCCATAACAT ATCTGCATGA TACAAAAATA 2400 GCTCTCTCCT CCACCAGATC TGTGAGTAAA ACTGAGACTC CAGAAAGCTG GGCCATGTTT 2460 ATCCTGGGGT CAGTTCCCCC AAATGCCCTG ACTTGTCTGT GGAGGAGACT TCACCTGGCT 2520 CAGTGCTGGT TCAGGTGGTC CAGGGCCAGC TGACTTGGGA AGCTCGGGGG CGTTCCCAGC 2580 CCAGGCTCTC AGGCCAGGCA GGGGCCATAA ACCCCCACAG CCCAGGCTCG GACCCACTGG 2640 AGGCTTTAGC CACCTGCAAA CCCTCACAAT GCCCCGACTC CCCACCGTGT GGCTGCTTCT 2700 ATGCCAAGAG GAGGAAGTGG GGGAAGAGAT GGGCTCTTTG GCCCCAGCGC CCGGGGGTGG 2760 CCTGCCTGCC TGCTGCCGCC AGGAAAGAGG GAATTTGGAG AGATTTCCGC TGCGGATGTG 2820 CCAGATAATA CAGCAGAGAG GCAGCGTCAA CAGGGCATGT GCCTGCCTGA CGAGATGTGC 2880 TTCCCCTCCT CCAACCACAA AGCTACCAGG GGCTGTCTCC AGGGCCCCGC CAGAGTTTCC 2940 AAGTGCTCAG GGGTCCCAGA GTTCATGAGT AGGACACCAG CAAGCCCCTG TGTTCTTCCT 3000 GACTTTATCT AGTTGGATTT CCTGGCATTC TAGGCGGGCA AGTGGGGACA GGGGTCACAC 3060 ACACTCAAAC ACACCCACAT ACACCAGATA CCTACTGTTC CTTAGCCAAC CAGCAAACTC 3120 CTATGCATCC TTTAATACCC AGCTTAAGCT CCTCTACACA GCCCTCCCAG ACTGCCCAAT 3180 TCCTGGCCCC CCGGCCCCCA TTAGGGCATC TATTAATCTT ATGTTTACCA AATAGAAATG 3240 GGCACTTCAT ACGTGTCTGG CACAATGCTG GGTGCTAGGA TGCGATGGTG AGACAGATAA 3300 ACACTGTTTC AGCTCCAGGG GAATTCAAAA CTTGGCTTTT ATGCTCCATT TGAAATTATT 3360 CCTGCATGTA TCAGGAGCTT CCGTGAGACC AGCAGCTCCT GAGGAGCAGG AATGGAGACC 3420 AATTTATCTG TGTCCCATGG CCCAGCGGTG CTCAGTTAAT GTTTGCTGAA TGGATGGACA 3480 GACAGATGGA TGGATGGATA GATGGGTGAG TTGGTGGGTG GATGGGTAGA TGAGTGTGTG 3540 GATGGATGGG TGGGTGGATG AATGGATGGA TGGGTGGAGG GGGGTATGAG TGGGTGGATG 3600 AATGGACAGA TGAATGGACA AATGGATGGG TGGGTTGGTG GGTGGACAGG TGGATGAGTG 3660 GATGGATGGA TGAGGGATGG ATGGGTGGGT 3690
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