Tag | Content |
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EnhancerAtlas ID | HS092-25752 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:235958890-235961040 |
Target genes | |
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) |
ATF3 | MA0605.2 | chr2:235959797-235959809 | GGTGACGTCATC | - | 6.74 | ATF3 | MA0605.2 | chr2:235959797-235959809 | GGTGACGTCATC | + | 6.92 | CREB1 | MA0018.3 | chr2:235959797-235959809 | GGTGACGTCATC | + | 6.74 | CREB1 | MA0018.3 | chr2:235959797-235959809 | GGTGACGTCATC | - | 6.74 | JDP2(var.2) | MA0656.1 | chr2:235959797-235959809 | GGTGACGTCATC | - | 6.92 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_47779 | chr2:235958899-235960840 | Pancreas | SE_65336 | chr2:235955936-235961717 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I235047 | chr2 | 235956418 | 235961326 |
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Enhancer Sequence | CTGGGACTAC AGGTGCCCGC CACCACACCC GGCTAATTTT TTTTGTACTT TTAGTAGAGA 60 CAGGGTTTCA CTGTGTTAGC CAGGATGGTC TCGATCTCCT GACCTCGTGA TCCACCTGCC 120 TCAGCCTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACC GCTCCTGGCC TAGCCCTGGG 180 TTTCTAGTAG CTTCTACAAA AACAAACGGC CACCAGGTCC TCAAACCCCC TTCTGGCCAG 240 CCTCGTTGGT AGCCAGCTGT CAGCCTCTCA TATCTAGGGA GGCATCAGAA TGATCTGTCG 300 CTCCTGGTTC TTTTTAAATT CCATGGATTG AGATGCTGGG GGCCCACCTA GAAGGATCGT 360 GAGTCACCTA CTCTGGCTAA TGCATGCCAC AAGTCGCCAA AAAGGTCACC TTTTTGTATT 420 GTTAGACTCC CCCCAGGTAA ACATAAAGTG TACATTAGAA TGCTCAGTCT AAAACAGCTG 480 GGCTCGCTTT GAAGTAAGCA GCCCAGCCGA CCGCATGAGC ACTAGCAAGA CGACCCTGCT 540 ATCGGCACAA AATAGTTGGC CAAAGAGCGC CGGTACCAGC GGTGTGGTTG GCGGGGGTGG 600 GGGGTTGTTT GTTTTTTAGC ACACTTTGGA GTCCTAAAAT GACAACCTCA GGTGCTGAAA 660 CAGAGCGTAG AGAGAAAGAA CGCCAGGACT GGTGACTTTC CTCTTCTCTT AGCAACTCGC 720 CTGTCCAGGG GCTCACGGGA GCCTCAGAAA CCGTCTCTGG GCTGCCTCAG GCCACTGTGC 780 CCTGGAAGCC AAGCCTTTCC CATTGTTGGA TGAGAGAAAG CTTTAAGGGT GGGGGTGAGC 840 TGTGCCTTCT ATGGCAGAGG AGACTCAGAC AAGAATCAGA CCCAGCATGC GGCTCTCCTG 900 CCTTCCTGGT GACGTCATCC TGACTGGCTC AGAGCCACAC GCTAACCATG TGTGGCCTCA 960 TTTATAATTA GGATGGCGCC AGAGTCGCTT GCATGACACC CAGTGGCAGT CATGTGACTT 1020 GGCACAGTGT ACAGGACTAG CAGGCCTGCT GTCTTGTGCT AGCCAATTTG ATTTGTTTCT 1080 TTAAACCAGA AGTGTGAGTT TGACCCCAGC CTGGGGTCCC CCAGATATAT TAGCCATATG 1140 TTCAATGCCT GTCCCATCCA GCCCCCGTTT TTAGGAGGGA ATTGAGTCCC AAGGCGGCCA 1200 CGTGGTTGTT CCAGCCTCAG CTGGGACTTC ACTGTCCCAG CAGGGCTGTC TGTCCTATTA 1260 CCTCCCCTCT GACTTCCTCT GTGGTTAGTA ATCCCTGTCC TAAAGACACA GTAGAAAGTT 1320 CTTGCAGCTT TGACGTGGGA GCAGTCCCAC CAATTGTGGA AACCGTTTTC TCATGTTGCA 1380 CAGTCCTGGG GGAGGTCTGT GCATCTCCTG GTCACCGTGG TTCTTGGTGG TACACCCTGT 1440 CTCTGACCAG GGCCTCTTCT GTTCTCTGTC TTCTTCTCCC TGGGTGGTCC CTGCCTGAGT 1500 CCCCCAGCCT TCTACCCGCG GTGCTCTCTA ACTGGCCAAT GTCAGCACCG CACACTCAGC 1560 AGGTCCAGCT CGCCCTCCAT CCGTCTCGGC CTCAGGCTAT GGTGTCTATT TGGTGAAATG 1620 CATTCGTTTC TCTCTGGTGT CCCCAGAGAG TGGGAGTGGT GACAACTCTA ATCCATATTC 1680 ACCCTGTCTG TTAGCTTCCT GGGGCTGCCA AGACAAATGA CCACAAACCA AGGGACATCA 1740 AACAACAGAC ACCTGTCCTG TCACCATTCA GGAGGCCACA GGTCTCAGTC AGGGGTCCCA 1800 GGGTGGCCTC CGTCTGGAAG CAGTGGGGGA GAAGGGGTTG CAGGCCTGCC TCTCCTAAGC 1860 CCCACTGGCT CAACCCTCCT TCTTTTCCTT GGCTTGTTGC CGCATCTGTC CCGTCTCTGC 1920 CTCCGTCTTC ACACGGCCTT CTTCTCTCTG CCTCTCTGTC TGCTTTCTCT TCTTATGAAG 1980 ACGCCAGTCC TTGGTGACTT CCTCTAATCC AGAGGGACCT CATCTTAATT CTATCTGCAA 2040 AGACCCCATT TTCAAGTAAG GTCACGTTCT GAGGTTCTGG GTGGATGTGG GCTTTGGAGG 2100 GAGACACTGG TGAACCTGGC ACGCTCTGCA CATCATCTCT TTTCTCCCGT 2150
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