Tag | Content |
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EnhancerAtlas ID | HS040-01097 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:27179360-27180210 |
Target genes | Number: 14 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:27179753-27179772 | CTGACACCAGGGGGCACCA | + | 6.89 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_23384 | chr1:27179734-27183526 | Colon_Crypt_1 | SE_24351 | chr1:27179889-27180833 | Colon_Crypt_2 | SE_26621 | chr1:27173970-27186608 | Esophagus | SE_33637 | chr1:27179787-27186622 | H2171 | SE_34025 | chr1:27179331-27180866 | HCC1954 | SE_34526 | chr1:27179715-27180968 | HCT-116 | SE_57686 | chr1:27180033-27180802 | VACO_503 | SE_64263 | chr1:27179011-27191692 | NHEK | SE_67095 | chr1:27179787-27186622 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I026852 | chr1 | 27178686 | 27182352 |
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Enhancer Sequence | GTGAGCGGGG TGCGGAAGAG GGGTAACAGG GCCATGCCTG GCCAGTGATC AAAGTGTTCC 60 TGGATATCAG CCGACCTCCC CCTACACCCT AGATGCCCTC CGTCCACTAC CCCCTGGAGG 120 GCATTTGTCA TGTGACGGAA TTCCATGGAG AATTGTTATT TAATCACGTG CTCATTGTAG 180 AAAAAAAAAA TTAAGTACAA AACGTAAAAC AGAGGAGCAT TGGATATGAC ATGTAATTCT 240 ACTCCCCGGG GGTAGCCACC ATGACTGTTT CAGCCATGTT TGAATGACAC TGCCCTTCCG 300 GTTGCCCACT GCCTGGACTG GGTGGCGACT CCATCCTCTC CTGGCAGTAG GAACCCTGGG 360 GACTCAGCCC TGCTGGGTCA CTCCCTGTTC ATCCTGACAC CAGGGGGCAC CAGAGTTCCA 420 GAACGGGGAT TACATTGCTG TGGGTACTGC TAAGACAAGT CATTCCCACA CAGTCATGTC 480 ACCTACCCCA CCCAGTATCC CTGTCACCCA GCCTGCCTAG AGGGGAAGGG AACATAGGAA 540 TTTCATAGTC ATCAAATACC TATTCATCCT TGCTTTCCTC CCTCACCTGC AGCCTGGCTT 600 CTTGGCAGCC AGACAGGTGG GCCAGTTGGA ATTAATAGTG AATAAATTCT GTGGCCAAAA 660 GCCAGGTGGC CAGAGGGCAG AGAGAGGCCT GCCAGAGGTA AGAGTCTTGG GCCCCCAGAT 720 GGGCAGCAGC TCTCCTTTCC TCAGCCTTTC TCAGCCTGGG CCTTTCCTTG GCTGAGATAG 780 ACTCTGCCGT CCAACCCCTG GCCTAGAGCC TCAGTGTTGG GCAGAGCCCT CATGTGTCTC 840 CCTTGTGTTT 850
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