Tag | Content |
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EnhancerAtlas ID | HS060-08982 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr12:130978900-130981160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr12:130980027-130980042 | AGGTCACCCTGGCTC | + | 6.03 | IRF1 | MA0050.2 | chr12:130979185-130979206 | AAAAAAAAAAAGAAAGAAAAG | - | 6.41 | Nr2f6(var.2) | MA0728.1 | chr12:130978967-130978982 | GAGGTCAAGAGTTCG | + | 6.24 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65722 | chr12:130980910-130982292 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I130496 | chr12 | 130980911 | 130982292 |
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Enhancer Sequence | ATGCAAAGCA CAGTGGCTCA TACCTGTAAT CCCAGCACTT TAGGAGGCCA AGGCAGGCAG 60 ATCACCCGAG GTCAAGAGTT CGAGACCAGC CTGGCCAACA TGCTGAAACC CCGTCTCTAC 120 TCAAAATACA AAAATTAGCC AGGCATGGTG GCAGGCACCT GTAATCCCAG CTACTCAGGA 180 AGCTGAAGAG GGAGAATCGC TTGAACCCAG GAGGCAGAGT TTGCAGTGAA CTGAGATTGC 240 CCCACTGCAC TCCAGCCTGG GCAACAGAGT GAAACCCTGT CTCAAAAAAA AAAAAAGAAA 300 GAAAAGAAAA GAAAGAGCAA AGTAGGAGTC AGGTAACCCA CGGAGGCCTC CAGGACCCTG 360 CACTCCAGCC CTGTGTGCTG GTTACTCAGG ACACACCCTC TTCCCTGCTG TCCAGAGCAC 420 TTGGCCTTAT GTGGGAAAAG GATGCATTTG TGACCGCTGG GTCACAAAGT ACCACAACTG 480 GCACTTCTGC TTAAGACAAT GGAAAGTGTC CTCTCACAGC CCTGGAGCAC AGAAGGCTGA 540 AATCCAGGTG TCGGCAGGGC CGGATCCTCT CGTGGAACCT CTGAGGGAGA AGCCGCCCCA 600 TGCCCCGCTC CAGCTGCTGG CGTGGCCACG ATGCTTGGTG ATCTTTGACC AGAAGACACC 660 TCACTCCCAT CCCCTTGGGT GTCTCTGTGC CTCTTCTTCT TATAAGGACA ACAGTCCTTG 720 GGTTTAGGGC CTGCCCTACT CCAAGATGAC CTTATATTAA TGACATCTGG ACAGACTCAT 780 TTTCAAATAA GGTCATATTC ACAGATACAT AGATTTAGGA CTTGGGCGTC ATTTGGGGGA 840 ACACAGCTGG CCCTCTACAT GCCCTGAAAT GATGAGGGGG GCTGCTTCAC TTGCTCCCCA 900 TCTGCCTGGA TTCATGCCTC TGGACACCTG CCCCAGACCA AGCCATCAGC CACGCTGGTA 960 CATGCCCTAG TGGCTCCCGC CTCAGTGCTG CCCGTTGTCT CCTCTTGCCC CTGTGAGATT 1020 TCCCCAGGGA TGTTGCTTGG TCAGGCCACT GTCATCACGT GGGCCTCAGC TGAAGTGTCA 1080 CCCCCTAACA GACATGTGCA GGGTGCCCTG CGCTCCCCTC TCCCTCCAGG TCACCCTGGC 1140 TCATCACCGT CTTCCTCCGT CTCTGAAATT CTTATCTATT TGCTGGATGA CCTGATTTTT 1200 TTTCTGAGCT CCTCCCACCC CAGTAGAAGG TAAGTTTCAT GAAAACAAAA ATAACCTTGG 1260 ACTTGCTCCT CGTTTTACTC CAAGCATCTG GCATGGTACC TGGCTATCCT TCTGTCTATT 1320 CTAGTAGATT CCTTTGAGGG TGTATATCAA TGAAATTGCT CACGGTATTA GCAATTCTTG 1380 ATCACTAACC TCTCCAGCAC CAGCCACTAT GTTAGATCAC TGGGCACATT CTATGCTTTG 1440 AACCCTTACA TCTAGAAAGG TACTTTATGG CCACTTTAAA GATGAGAGAA CACCCCGGTT 1500 CTCAGAAATT AGTTAGCTTG ATCACACGTA AACAACTAGT TAATCATCAA ATTCAAATTT 1560 GAACTCAGAC TGGTCTAACT AAAAGCCCAA AGTCTTTGAA TTAGGTCATG CTACTGAGAT 1620 CAACGGGAAC GTCCCCCTAG GGTGGGTGAT GATTCTGCCG CTGACTCATT GGACCTAAAC 1680 TGTAAAGCAT TGTGGACCAC GGCAGAGAGT ACGTCCGTGC CTGTAGCCAT GTGATACGGT 1740 TTGGCTGTGC CCCACCCAAA TCTCATCTTG AATAGTAACT CCAGTAATTC CCATGTCTTG 1800 TGGGAGGGAC CTGGTGGGAG ATAATTGGAT CATGGGGGCG GTGTCCCCCA CACTGTTCTG 1860 TGGTAGTTAA TAAATCTCAC AAGATCTGAA GGTTTTATCA GTGGAAACCC CTTTCTCTTG 1920 ATTCTCATTC CCTTCTCTTC TCTTGCCTGC TCCCACGTGA CACATGACTT TCACCTACCA 1980 CCATGATTGT GAGGCCTCCC CAGCCACATA GAATGGTGAG TCCATTAAAC CTCTTTCCTG 2040 TATAAATTAC CCAGTCTCGA GTATGTCTTT ATTAGCAGCA TGAAAAAGGA CTAAACCACC 2100 ATCTCACTGT CCTCACTCCG GTCTCAGCAG CCCTGCTGAG CAGCTCTGGG GTAGAGGAGG 2160 CTGCGAGGGG TGAGGCTCCA TCCACTTCCT GCAGGAGGGA TGCTTCTGTC CACGGGAGAC 2220 CAGCACACAG TGATACCTCA TGAAAGGCCA CGTTCCCATC 2260
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