Tag | Content |
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EnhancerAtlas ID | HS036-00062 |
Organism | Homo sapiens |
Tissue/cell | endometrioid_adenocarcinoma |
Coordinate | chr1:16501970-16503740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr1:16503374-16503391 | TGCTTCCTAGGAAGTGA | + | 6.08 | RREB1 | MA0073.1 | chr1:16502026-16502046 | TGTGAGGGGGTGGGAGGGGG | - | 6.61 | RREB1 | MA0073.1 | chr1:16502036-16502056 | TGGGAGGGGGTGGGATGGGG | - | 7.16 | SOX10 | MA0442.2 | chr1:16502839-16502850 | TTCTTTGTTTT | - | 6.62 | ZNF263 | MA0528.1 | chr1:16503057-16503078 | CATCCTCCTCCATCCTCCTCC | - | 6.3 | ZNF263 | MA0528.1 | chr1:16503060-16503081 | CCTCCTCCATCCTCCTCCTCC | - | 8.07 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_23091 | chr1:16501962-16502745 | Colon_Crypt_1 | SE_23091 | chr1:16502844-16503560 | Colon_Crypt_1 | SE_23751 | chr1:16502050-16502674 | Colon_Crypt_2 | SE_23751 | chr1:16502855-16503434 | Colon_Crypt_2 | SE_24743 | chr1:16497841-16502803 | Colon_Crypt_3 | SE_24743 | chr1:16502816-16503501 | 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 | chr1:16502024-16503485 | HMEC | SE_38062 | chr1:16499064-16503878 | HUVEC | SE_40833 | chr1:16501759-16503971 | Left_Ventricle | SE_44998 | chr1:16502053-16503662 | NHLF | SE_46140 | chr1:16501795-16503844 | Osteoblasts | SE_47009 | chr1:16502010-16502676 | Ovary | SE_47009 | chr1:16502860-16503560 | Ovary | SE_47150 | chr1:16499250-16512083 | Panc1 | SE_47539 | chr1:16501964-16502662 | Pancreas | SE_47539 | chr1:16502819-16503601 | Pancreas | SE_48744 | chr1:16501448-16503785 | Right_Atrium | SE_50427 | chr1:16497958-16504232 | Sigmoid_Colon | SE_52536 | chr1:16501918-16504326 | Small_Intestine | SE_56795 | chr1:16499345-16504738 | VACO_400 | SE_57357 | chr1:16501943-16502709 | VACO_503 | SE_57939 | chr1:16501961-16502682 | VACO_9m | SE_57939 | chr1:16502843-16503425 | VACO_9m | SE_64726 | chr1:16502266-16503212 | NHEK | SE_65472 | chr1:16501980-16503977 | Pancreatic_islets |
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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 |
GH01I016171 | chr1 | 16497941 | 16511884 |
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Enhancer Sequence | GCCTGGGTAT GTGGGGCTTA GGCCAGAACA AATCTTGGGA CTGAGTGTAA AATATATGTG 60 AGGGGGTGGG AGGGGGTGGG ATGGGGCTCG GTGCGGGCCT GGCAGGTGTG CTGGGAGGCA 120 AGGCCTATGA CTCCTGTGGG CCTGCTCTTC CTCCCATCCC ACCCTCCACA GTCCCCACCT 180 CAGGGGCCCT GGGCCTGGGG CAGCAGGGGC CGGGATGTGT CTCTCCAGAG CAGGAACGGA 240 GGGGCCTCCG CAACTGGTTG GGGAGGGGGG GTGGATGCCA GCCCCCGCTG ATTAGGTCTC 300 AAATTAAAGC CGAGCTTGCT CCTGTCGCTG CTCAGGCAGG CCCTCCTCCT GGCCACAGTT 360 CCCTGCCTGG CCCTCTGCTT CGGGCCTCAT GGTGGCTGGT TGCTCCCAGC CTAGAATTGC 420 TAAAAGGCTC CCGTAGTGGG TAGGAGCCTC AGGGGACCTG GGAGAGGCTT CAGGGGCCCT 480 GCCTGTGCGG GGGTCTCTCC TGTGACCCTC AGACCTGAGC CAGTGTCTGG GGACAAGTCA 540 CCGTGTCAGA GGCTGCGGAG AGCAAAGCCC AGGCGGTGAT GACTTGAGTT TCCAGGCCGG 600 GTGCCAGGAG GCCCGCGGTC ACACTCCGCC TGGGGCCTGG GCTCCGGCCA ACTGTCAGCA 660 GCAGAGATTG TTGGGTTGGT TTTATTTTAA ACAAAAAAGA ACTTTGAGTG GAAACATGTG 720 TTTCTTTTTT CTCCCCCTTC CCTCTCTCCC TATCTCTCTC CATCTCATCA TGGAATATTT 780 CTCTTTTTTG TACCTCCCTT TCTCTGTTTT TCTCTCTGTC TTCCTCTATT TGTCCCTGCC 840 TCTGTCTCTC TCTCTCTCTC TCTCATTCTT TCTTTGTTTT CCTATCTCTT GATTTCTCTG 900 TCTCTTTCTC TATTTCTTTT TCCGCAGCTT TCAGGAGTCA GGAGAGGTAC CAGACTTCCT 960 CCCTCGGGGT GTGGCCTGGG CCCCTGCCAT AAAATCCCCA GGCGTGCCAC GGCCCTATGT 1020 CGGGGGTCTG CCGCTCCAGG GGAGGGAGGG GGTGTCTAGC AGCGGAGGCT CCAGGACCCA 1080 AATGCTCCAT CCTCCTCCAT CCTCCTCCTC CAAGCTCCCA CTGCCCCTGC ATCTGCCCTT 1140 CCTGTGTCTG TTTTCTCTAC TAAGCATCTA GAAAATAATT CTGCAGCTTG AGACAAGTTT 1200 TAAAACACTG GTCTGGCCCA AACCACCCAT CTACAGCCAG AGACTGGCGC CGAGGAGGGG 1260 ACCATGGCCT GCTCAACACC GCACGGAGGG TTAGGGGCAA AGCCAGGCCG ACCCAGGTCC 1320 CCCACTCCCA AGTGACATTA CTGACACCCC CAAACCCACA GTCACCACAC TTCTCAGGTC 1380 CCTGCGTCTT TCAGAGGGGT GGTCTGCTTC CTAGGAAGTG ATGTGCCCTC CCCTAAGGTG 1440 GTCACCCAGC ACAAGGGTCC CCCTGGAAAA TGTCCTGCCT TGGCTGGTCA CCCCTCCCCC 1500 AGGACAGACA AGCTTTTGGG CCCCCACCTT TCAGCCCCTT CTGCCAGGCA GTAGAGAAGA 1560 GAGAAGAGAG ACTCGCAGGC ACAGTGGCTC ATGCCTGTAA TCCTAGCACT TTGGGAGGCC 1620 GAGGTGGGCA GATCACAAGG TCAGGAGATA CAGAAGAGAG ACTGGCCACC CATGCACTGG 1680 GCCCAGGTCC TAGCTCGACG TCTGAGTCCT TGTGTGACTG TGAATATGAC TTTTCCACTG 1740 GCTGGCCTCA GTTTCCCCAT CTTTGTAACA 1770
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