Tag | Content |
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EnhancerAtlas ID | HS118-00272 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:24875320-24877520 |
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) |
Foxd3 | MA0041.1 | chr1:24875798-24875810 | GTTTGTTTGTTT | + | 6.32 | STAT1 | MA0137.3 | chr1:24876538-24876549 | TTTCCTAGAAA | - | 6.14 | Stat4 | MA0518.1 | chr1:24876535-24876549 | TCTTTTCCTAGAAA | - | 6.1 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29333 | chr1:24875714-24876651 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I024549 | chr1 | 24875715 | 24876651 |
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Enhancer Sequence | AAGGAATTCT GTGTTTAAAA ATGTAGTTTT CACATAGTTT AGGAAGTAGA AAACGTACAG 60 GGGAAATTTC ACAGTGGATG GTAAAACACA TGGAAGAATG AGGAACCTGG CATGATGGGG 120 AGGAGAGAGG TCCGGTAAGG GAACGAACAC ATAAGAAAAA AGCAGAGAAC GCAGCCTCTG 180 TGTCTCTCGC AGAGCCCAGC TCAGTGCCTT GCCCACTTAA GCTCTCAGGA AGTGTTCACT 240 CAAATGAACT CACGCATGTG TCTAACTGAG CGAACACCTG TATATCCCAG AAAAAGTAAC 300 TTCCAGTCCC CATAGAATAA GTTTAATAAA ACTCAATCCT ACAGCTCAGG AAGAACTTTC 360 TAAAAGCAGG ACAGTGGTTT TCCAAATGCC AGATATTTTT TCAGAAATTG TGTTTTGTTT 420 TTTGTAATTG TGATCATTTG ATTATTTGTT AGACAAACCT GATCACAGTG GTTTTTTTGT 480 TTGTTTGTTT TTGAGACAGG GTCTCGCTCT ATCACCCAGG CTGGAGTGCA GTGATGCAAT 540 CTCGGCTCAC TGCAACCTTT GTCTCCCGGG TCCAAGCGAT TCTCATGCTT CAGCCTCCCA 600 AGTAGCTGGG ATTACAGGCA TATGTCACTA TGCCCAGCTA ATCTTTGTAT TTTTAGTAGA 660 GATGGGGTTT CACCATGTTG GCCAGCCTGC TCTCAAACTC CTGACCTCAA GTGATCCACC 720 CACTCAGCTT CCAAAAGTGC TAGGATTACA GGCGTGAGCC ACTGCACCTG GTCATGTGAT 780 CAGAGATTTT TAATTGCCAG AGATGGCCCA TTGGCTCCTT TTGGCTTTTT GCTTTCTTTC 840 TTTTTATTTA TCTTAAACCA GCCTCAAAGC CCCCACTGTT CTCCTGAAAG GAACTGAGGT 900 GAGGAATCTA CCTCCTAAGG CAAATGACCA GAGCAGAGGA CAGGATAGAC TGGGTTTCCA 960 TCACGTTGAC ATATTATTAT CTTTCATAAC TGGGATCCTT TTGGATCATT AACAGTAGCC 1020 ATGAGGTAGA AGGTGGGACT AGACTCTGGA GGGGGACTTG GATGCTGAAT CAAACTGAGG 1080 AGTAGTTAAA ATAAGGACAG GGCAGAAGCA GCTTTCCATG AGATGCACCC ACCAGTGTTC 1140 CATGTCAGCT AACCCAACAT CCAGGAGTTA CCTCCCCTTT CCATGGCAAT GACCCAAAAA 1200 CCCAGAAGTT ACTACTCTTT TCCTAGAAAT TTCTTCATAA ACCATCCCTT AATCTGTATG 1260 CAATTAAAAG TAAGTATAAA TGGCCAGGCG CAGTGGCTCA CGCCTCTAAT CCCAGCACTT 1320 TGGGTGCCAG CCCTTGAGCA AGTCATTCCC TCTCTATGAT CTTGGGCTCC TCAGTGGCTC 1380 CCAACCCTGG TCACACATTA GCATCACCTG GGCACCTCAT AAAAACCCAT GACTGGTCTG 1440 GCCTCACTGC AGAGCCTCTA GCTCTATGGC TGTAAAGTGC AACCTTAGCA GAGTTTTCCA 1500 AAGTCCCCAA GGGATTCTGA GGGACCACCA GGACTGAGAC ACCCAGGGCT GGGGGATGTC 1560 CGAGTTCACC CAAACTTGGT TTCTCACTCC CTGGATTACC CCATTTCCTG GGCCTTTAGA 1620 ATTACTGTAA ATGCTTTCAT TTAACACAAT GTCCATCTAT AATACTATAA TTAATCTTGA 1680 TATTTGCACA AGGGTGTATG CAAATATCAA GAGTAATTAC TCTTTGTGCG TGTGCATGTG 1740 CGTGTTGTTG TTGTTGTTTT TGAGACAGAG TCTCGCTCTG TCGCCCATGC TGGAGTGCAG 1800 TGTTGTAATC TCCGCTCACT GCAGCCTCCA CCTCCCAAGT TCAAGCGATT CTCCTGCCTC 1860 AGCCTCCTGA GTAGCTGGGA TGACAGGCAC CCGCCACCAT GCCTGTCTAA TTTTTGTATT 1920 TTTAGTAGAG ACGGGGTTTC ACTATGTTGC CTAGGCTGAT CTCAGACTCC TGGGTTCAAG 1980 TGATCCGCCA GCCTCGACCT CCCTAAGTGC TGGGATTACA GGCGTGAGCC ATCATGCCTG 2040 GCCTACTCTT TGAAAGTAAG GTTATAAACT CATTCATGCT CCACGCCTTT TGGGGTAGGC 2100 AGATATCACT ATCCCAGCTT CCCTTTATTT TTCTCCAAAG CACTTATTAC TTTCCAACAT 2160 GCCATATCAT TGGCTTGTTT ATTTATTTAT TTGAGACAGG 2200
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