Tag | Content |
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EnhancerAtlas ID | HS095-19792 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr22:40413330-40415170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr22:40414140-40414151 | AATGACCTTGA | - | 6.32 | Esrrg | MA0643.1 | chr22:40414141-40414151 | ATGACCTTGA | - | 6.02 | RORA | MA0071.1 | chr22:40414142-40414152 | TGACCTTGAT | - | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_23648 | chr22:40413400-40414439 | Colon_Crypt_1 | SE_24534 | chr22:40413477-40413789 | Colon_Crypt_2 | SE_27100 | chr22:40413382-40414529 | Esophagus | SE_27100 | chr22:40414669-40416421 | Esophagus |
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| Number: 2 | ID | Chromosome | Start | End |
GH22I040017 | chr22 | 40413383 | 40414529 | GH22I040018 | chr22 | 40414670 | 40416421 |
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Enhancer Sequence | GCAATGAGCG ATTCTCCTGC CTCAGCCTCC CCAGGAGCTG GGATTACAGG TGCCCACCAT 60 CATGCCTGGC TAATGTTTGT ATTTTTAGTA GAGACAGGGT TTCACCATGT TGGCCAGGCT 120 GGCCTCAAAG CCCTGACCTC AAGTGATTCA CCCGCCTCAG CCTCCCAAAG TGCTGGGATT 180 ACAGGCGTGA GACACCATGC CTGGCCCTGC ACTCAGCACT TTCATGGTGC ATCTCACTAA 240 GTCCTGGGAC AACCCTTTGA GATAGGTGCA GTTATTAGCT CTATTTTGCG GCCAAAGAAG 300 CTTGGGCCGG CTGTGGCATG GGGATACCAG CCTGGTCTGC CTGACTTTAG AGTCGGTGCT 360 TTCAGTTTTG AAGGCAAACC GACTTCCTGG ACTGTATAGC AGTTACTGTT TACTGAGGAC 420 TTATTACATG CCAGAGGTTG TGTTTGCTGC TTTACCAAGT TATCCCTAAT CCTCAGGGCA 480 AAAGTGTAAA ATACAAGGTA TCCTCACTTT GCAGATGAGG AAACAGAGTC TCATTAAGGT 540 TAAGTGACTT GCCTAAGGTC ACAACTAGGA AGTGGGGGAT CCACAGTTAA AACAAAATCT 600 CTCCGACCCC AGAGCCGAGG ACTTTTCCTC AGCATCACAC GCAGGGTGTT TGGGCCAATA 660 AGAAAGCCTT CAGCTGGAGC GTGGAGCATG GTTTGTGTAG GAAGCTGGAA GTAGCTGTGG 720 TTAGAAAGGT GGAGCTGCCT CAGGCTGCAT AAACCTTGCC TTCCAGGGTG GATAATCAGG 780 ACTGATTTTT GTAAATGAAG GGTCCTGAGC AATGACCTTG ATTTGAGGAT GGCGTAGGAT 840 GGGATGGACA CCTGAAGGCC AAGGGAATCC AAGCCAGCCG GAGCTCTGCC TGGATCTGTG 900 CCTGGGGAAG CACAGAGCTT CGCACAGCTG CAAGGCCATC AGCGCATCCA GGCCTGCTGA 960 GAAAGTGATG TTTGAGCAGA TGTGTGGCTC ACGGAGATGA GCCCACCCCT GGCATCTCCG 1020 TGATGGCATC TCCTTGTGCC TGCTTGTTTT TCTAGGGTGT CAGGAGCAAC TTTCCTCAGG 1080 CCCCTAGATC TCCCATGATA TGGCTTCTTT ATTCCATTTT ATTTATTTAT TTATTTGAGA 1140 CAGTCTCTAT CACCCAGGCT GGAGTGCAAT GGCACGATCT CGGCTAACTG CAACCTCCAT 1200 CTCCTGGGTT CAAGTAATTC TCCTGCCTCA GCCTCCCCAG TAGCTGGCAT TACAGGTGCC 1260 TGCCACCACG CCTGGCTAAT TTTTTTTTTT TTTTTCGCTC TTGTTGCCCT GGCTGGAGTG 1320 CAACGGCGCA ATCTTGGCTC ACTGCAAACT CTGCCTCCAG GTTCAGGCAA TTCTCCTGCC 1380 TCAGCCTCCC AAGTAGCTGG GATTACAGGT GCCCGCTACC ATGCCCAGCC CATTTTTTGT 1440 ATTTTTAATA GAGGGTTTCA CCATGTTGGC CAGGCTGGTC TCAAACTCCT GACCTCAGGT 1500 GATCCACCTG CCTTGGCCTC CCAAAGTGCT AGGATTACAG GTGTGAGCCA CCTTGCCTGG 1560 CCCTGATACA GTTTCTTAAG AGCTGCTGGA AGACCCCCAG GATGGGGAGG TGGGGATTTG 1620 TCCAGGATGA AGTACAAGCA CACGGCCTGC ACCCCCAGGC CCATCTCCAG GGCTCAGATA 1680 TGCTCAAAGA TCGGGGGACG TGGAACTCCA GGAATGGTAC AGGTGGAGTT TTTGACTCTT 1740 GGCCACCAGT GACCCCAGGG CGAGGTGGTA CCATCTGAGC AGGGCATGCC TCTGTGGGCG 1800 TGTAGACACC GTGTGCCTCA CCAGTGCCTT TCCCCACCCA 1840
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