Tag | Content |
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EnhancerAtlas ID | HS101-02382 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:116895200-116896670 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2A | MA0003.3 | chr1:116896457-116896468 | AGCCTGAGGCG | - | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_28411 | chr1:116894511-116896360 | Fetal_Intestine | SE_29219 | chr1:116894416-116896665 | Fetal_Intestine_Large | SE_68278 | chr1:116891785-116921287 | TC32 | SE_68497 | chr1:116891900-116921072 | TC71 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I116352 | chr1 | 116894647 | 116896260 |
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Enhancer Sequence | TCAGTTTTGC AAGATGAAGA GTTTTGCAAG ATGGATGTTG GTGACGGCTG CACAACAATG 60 TGAATGTGCT TAACAACACC TAACCATTCA CTTAAAAAGC GTTACCAGCC TGGATAACAC 120 AGTGAGACTG TGTCTCTACA AAAAGAAAAA CCCAGCTGGA TGTGGTGGTA CACACCTGTA 180 GTGTCAGCTA CTTGGGAGTC TGAAGTGGGA GGATTGCTTC AGCCTGGGAG ATCCAGGCTG 240 CAGTGAGCTG TGATCTTACC ACTGTTTTCC AGCCTGAGCA ACCAAGAAAG ACCCTGTCTC 300 ATTAATTAAA GAAAAAAAAA TGTTTTAATG GTTACTATGG TAGTTTTTTT TTTTTTTTTT 360 TTTGACACAG AGTTTCACTT TTGTCGCCTA GGCTGGAGTG CAATGGCATG ATCTCGGCTC 420 ACTGCTACCT CTGCCTCTCT GGTTCGAGAG ATTTTCCTGC CTCAGCCTCC CGAGTAGCTG 480 GGATTATAGG CATGCACCAC CATGCCCAGC TAATTTTGTA TTTTTAGTAG AGACAGGGTT 540 TCACTATGTT GGTCAGGCTG GTCTCAAACT CCTGACCTCA GGTGATCCGC CCTCCTCGGC 600 CTCCCAAAGT GCTGGGATTA CAGGCCACTA TGCCCGGCCT GGCCTTCGAA TATAAAAAGT 660 CATGATATTT CCCCTTATCC TTCTTTCCAG GTGAACCATT CCAGTGACCA TTAACTATTT 720 CTTTGAATGA CATGATTTTA AATTTTCATC ATCCTGGACT TCCTACTCTC CCCGCCTTAA 780 AGATGATGCA ATAGTAATCA CTGTATGACA GTAATAAATA CTTACTGAAT GCTTGCTCTG 840 TGTCAAGCAC CGTGCCAACC TTTGTACATA AATTGTTTCA TTAATTATTA TAACAAACCC 900 GTGAGATAGA TGTTATTAAC TGCATTATGT GTAGATGAGG AAACTGAGGC ATAGAGTGGT 960 AAAAGAACTT GCCACGATCT TACAGCTAAT GAGTGGCAGA GCCAGAATAC AAACACAAAG 1020 AGTCTGGTTT CGGAGCCTTC TTTCTTAGTC ATCTCCTAAA AAAACACACC TATTCCATTA 1080 AATTCAAGAA AAGTTTGTTT TAATAATTTA ATAGAAAAAA ACACATATTG TATGATACCA 1140 TTGTGCAAAA TCATTTCTCT CTCATTACCT CTCTGTTTGT GCCTGTCAAT GTGCATTTTA 1200 AAAATATCTA GAATGTCCAG GTGTGGTGGC TCATGCCTGT AATCCCAGCA CTTTGGGAGC 1260 CTGAGGCGAG TGGATCACCA GAGGTCAGGA GATTGACATC AGCCTGGGCC AACATGGTGA 1320 AGCCCCATCT CTACTAAAAA TACAAAAATT AGCTGGGCGT GGTGACAGAC ACCTGTAATC 1380 CCAGCTACTC GGGAGGCTGA GGCAGGAGAA TTGCTTGAAC CTGGGAGACA GAGGTTGCAG 1440 TGAGCTGAGA TCACACCACT GCACTCCAAC 1470
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