Tag | Content |
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EnhancerAtlas ID | HS158-00663 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr1:16499550-16501750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr1:16500147-16500162 | CTGCTGACTCAGCGC | - | 7.07 | MAFF | MA0495.3 | chr1:16500147-16500162 | CTGCTGACTCAGCGC | + | 7 | Spz1 | MA0111.1 | chr1:16499568-16499579 | AGGGTATCAGC | + | 6.32 | TFAP4 | MA0691.1 | chr1:16501598-16501608 | ATCAGCTGTT | - | 6.02 | ZEB1 | MA0103.3 | chr1:16500289-16500300 | GGGCAGGTGGG | - | 6.14 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_23091 | chr1:16499347-16501823 | Colon_Crypt_1 | SE_23751 | chr1:16499364-16501671 | Colon_Crypt_2 | SE_24743 | chr1:16497841-16502803 | Colon_Crypt_3 | SE_26540 | chr1:16496436-16504779 | Esophagus | SE_28102 | chr1:16497879-16504574 | Fetal_Intestine | SE_29455 | chr1:16497964-16506131 | Fetal_Intestine_Large | SE_31527 | chr1:16499336-16504399 | Gastric | SE_34268 | chr1:16497740-16504248 | HCT-116 | SE_34628 | chr1:16497415-16506115 | HeLa | SE_36144 | chr1:16498765-16501519 | HMEC | SE_38062 | chr1:16499064-16503878 | HUVEC | SE_44998 | chr1:16499693-16500212 | NHLF | SE_46140 | chr1:16499323-16500582 | Osteoblasts | SE_47150 | chr1:16499250-16512083 | Panc1 | SE_47539 | chr1:16499523-16500148 | Pancreas | SE_47539 | chr1:16500355-16501118 | Pancreas | SE_47539 | chr1:16501350-16501756 | Pancreas | SE_48744 | chr1:16501448-16503785 | Right_Atrium | SE_50427 | chr1:16497958-16504232 | Sigmoid_Colon | SE_52536 | chr1:16497970-16501408 | Small_Intestine | SE_56795 | chr1:16499345-16504738 | VACO_400 | SE_57357 | chr1:16499350-16500174 | VACO_503 | SE_57357 | chr1:16500236-16501136 | VACO_503 | SE_57939 | chr1:16499369-16500862 | VACO_9m | SE_64726 | chr1:16499137-16501292 | NHEK | SE_65472 | chr1:16498579-16501949 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 16499607 | 16500371 | chr1 | 16499761 | 16499895 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I016171 | chr1 | 16497941 | 16511884 |
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Enhancer Sequence | CCAGCCGAGG TCACTTGAAG GGTATCAGCC CTGAGGAGGA GTTCACGGGG CCTCTTCCTC 60 TCGGCCAACC CCAGCAGAGC TTGGAAACTG AGGCCCAGAG CAGGAGTCCA GGCTCATAGA 120 GCCGGCCTGG CAGAGGAGGG GTGGGGGAGT TGCGTCCCCA CCATTCCCAC TGGGGCATAC 180 AGCGCCTTTC TGAGCGTCAC AGGCCTGTCT GTGTCCTTCT TTTGCGGAAG AACTAACCAC 240 ACCTCAGGTT CCCCTTATGA AAGACAGAGG CTGAGGAGAG TGAGTCAGTT TTATTATATG 300 AGATAAGGCG GCTGGACAAA GCAGCGACAC AGGGACTGGC ACACAGACAG TGCTCAGCGA 360 AGCAGTCGCC TTCCTTCAGG TCTGAAATCC TCACTCAGCT CCCCAGCTTC TCTGGGGGAT 420 CTCCCTTCCC CTCTCTGGAC CCCTGGGCCT GACTTCCCCC ACTACTCCCA GCCTTTGTCC 480 CACTCCTGCC CCAGGCACCC CTCCCTCCTT CATGGGAAAT GGAGCTTCCT CCTCTGGTCC 540 TGCCACCACC TTCCTGGTGA GGGTCGGGCT CTGCTGGGAG TGCCAGAGCT GCCCAGCCTG 600 CTGACTCAGC GCCTGGGGAT AGGGCTTGCT TTAGGAACAG CCCAGGCCTC GGGCAAACAG 660 AGCCACGGCA ACCACACCCC TGCCACAGGA ATGCAGCAAC ATTCCTGGGG GGTGCCGTGG 720 CACCGTGCCT GTGACTGGGG GGCAGGTGGG GGGCAGGTAG ACACCTGCCT CTGTTACCTT 780 GCCACAGGTA GAAGGGAGCC AGGAGTCAGG GCCCAGTGTC CTGGGGCAGG GGGATGGAGT 840 GAGGTCATGA GGCTTTGAAA TCTGTACCAG CCATGTGACT TGAACAAGGC CTCTCTGAGC 900 CTCAGTTTCC TCACCTGTAA GGTGAAGGGA GAATAGCGGT AGCCTTCTGG TGGGCTTATG 960 GGGAGGACTG AACGAGAGTG CGCCCGTCTG GGGCTCAGCA TCAGCCTGCC TCACCGTGAG 1020 GATTCCGTGA AGCAGACCCT CACCCCTGTA ATAGAATCAG GGGGTCTTCT GGCTCTGGGC 1080 CCTAGAATGG GGCTGAAGCC CAGAGAGGCA GTTGCACCTC CCCTAGGCCA CACAGCAGGT 1140 ATAGGCCCCA GGGGCTGAGT GCCCATCATG CCTGCCCTCC TCTCCATCCA CCCAGAGCCT 1200 CACTAGCCAG ACCCGCACTC TCCCATCCCC TGGGCAAGTC TGCACCCCAG GTCGGTGAGG 1260 ACTCCCAGAT TCTACTCCCA CCAGCCAGGG CCAGACCTGG TGCAGGAGGC TCCACAGTTC 1320 TCCTGCTCGG GGCTCCGTCT CCCCACTTCC TGGAGCTCCA TCCAAGTGGG GAACCCTGCC 1380 CGTCCTCTGC CCCTCAAGCC AACCAGGCAT TTACGGGGGA TGGGGCAGGG AGGGAGGCCA 1440 GGACCTGCAT CCTTCCAGCC CTGGCCCTCA GCAACCCCAT CAGGCAGTCA GGGGAGGAGC 1500 CTCCCCCAGG GAATCCTCCC TCCCTCTGTG TTGGCCTGGC CAGGTTCTCC TCTCTCTGTC 1560 TGCCTTTGTC TTTTTCTCTC TGTCTCTTCA TCCCAGGAAG AGGCCACAGG ACAGGGGTGT 1620 CCCAAGCACA GAAGAAACTT GTCTGATGAA AACAGGCCTT GGCTGGGAGC AGGGCCATCT 1680 GGATTTGCAC CCTGATTCTG TCTGACTTGC TGTGTGACCT TGGGCGAGTC CCCTCCCCTC 1740 TCTGGTCTTT CCCATTATTA TCTACCCAGC ACATAGTAGG TTCTCGGAAA AGGGGAGTCA 1800 CATATGCGTG CCCCCAGCTC TCAGCCCCTC ACTGCCTCCT TTAATCCCCA CAGATCTGCC 1860 AGCCTTTGAT ACTCCTGTGG GTGGCCGAGC CGGGGTTCTG AATAGGAAGC TGAGGGCTCA 1920 TGGGCTGCGG GGAAGCAGGC AGGGGCTGAG CCTGCCAGGC CTGCCCGAGG GAGGGGGCTG 1980 TGGGCCCCTC GCCATTCACT GCTAAGCCTG GATCCGGGCG CCTTTGTGCC AAGAACAAAA 2040 CCCGGGGGAT CAGCTGTTCT CAGGCCTGCC TCTCTCAGCT CCGGAAGGGA CGGAAGCCTG 2100 GGCCTGAGGG GTGGGCCGCA CTCCCTCCAT GGGCCCTGGG GTGCCGGGGC TGGCCCCATA 2160 CCCCAGAAGC TCCCCACTAC CTCCGGGTGT GGAGCTATGG 2200
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