Tag | Content |
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EnhancerAtlas ID | HS158-00349 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr1:9361660-9363500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr1:9362643-9362658 | TGGCCTTTGGACTCT | - | 7.58 | USF1 | MA0093.2 | chr1:9363465-9363476 | ACCACGTGACC | + | 6.32 | USF2 | MA0526.2 | chr1:9363463-9363479 | CAACCACGTGACCAGT | - | 6.1 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_00563 | chr1:9361755-9364768 | Adipose_Nuclei | SE_01570 | chr1:9359845-9363523 | Aorta | SE_23490 | chr1:9362746-9363598 | Colon_Crypt_1 | SE_23818 | chr1:9362895-9363370 | Colon_Crypt_2 | SE_26458 | chr1:9361668-9364426 | Duodenum_Smooth_Muscle | SE_26667 | chr1:9361744-9363493 | Esophagus | SE_32227 | chr1:9362378-9363428 | Gastric | SE_45049 | chr1:9362570-9363503 | NHLF | SE_50208 | chr1:9361719-9363620 | Sigmoid_Colon | SE_52461 | chr1:9361723-9363621 | Small_Intestine | SE_65576 | chr1:9362424-9363473 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I009298 | chr1 | 9358616 | 9364232 |
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Enhancer Sequence | GGTAGGATGA CCTAGGTGGA TTCTCGTCAG CCTCTTTCCC TGGCCACCCC TGTCATCGCC 60 TGGTGGGCTC AGGAACAAAG TGGTCATGGT GGCAGAGATG GAGGTGATGC ATGGGCTCAG 120 CAGCATGGAC TGCCACTCAC CAAAGCCGAC CTGGCTATGG CTACCACTGG CTGCTAGTCT 180 GCCAGAAGCG GAGACTAACA CTGAGCTCCA GTATGGCCCC ATTCCCCGGG ATGATCACTG 240 CACCTGGTGG AAGGCACATT GGACCACTTC TGTTTTGGAA GGGGCAGCGT TTTGTCCTTA 300 CTGGAGCAGG CACTTATTCT GGATACAGAT TCGTCTTCCC TGCACACAGT GCTTCTGCCA 360 AAGTCACCAT CCATTGATTG ACAGAACACC TTTCCCACTG TCACGCTGTC CGTGTAGCAC 420 TGCTTCCAGG GAGCTCACTT CACAACCAAG GAAGTGTGGC ACTGGGATCA TGTGCAGGGA 480 ATTGGCCGGT GAGCACGAGC CCACTGGTTT CGCCTATCAT GCTAAGTGGA ACTACGGTCT 540 TGTTATTGCC TTTATTTGGA AATTAAGTAT GGTTTAAGAA GATGCCAGTG GGTGCCTATG 600 GGTGCCAGTT GGTAAGGGGT GGACCTGTGA TGATTGATTT TGGATGTCAA CTTGACTAGA 660 TTAAGGAATA CCCAGGTAGA TGGTAAAGCA TTGATTATTC TCTATGCTTC AGTACACACT 720 GAGCCTGTCC CTTTTCTGCT GACAGGGAAG CCCAGTGGTT TGACATTGTG TAGAATGATC 780 GGGCTGCCCC AGATGTGTCT GTGAGGGTGT TTTTGGAGGA CACTGGCAAT TGAGTCACTC 840 AACTGGGTGG GGAGGATCTG CCCTCCATGT GGGCAGGCAC CATCCAGTCA GCCGGGGGCC 900 TGGAAGAAGG GTGAATCCTG GCTCTCTGTC CCGGAGCTGG GATGCTCTTC TCCTGCGCTT 960 GGATGTCAGA ACTCCAGGTT CTCTGGCCTT TGGACTCTGG GACTCGTACG AGTGGTCTCC 1020 GGAGTCTTTG ACCTGGGACT GGGAATGACC ACGTTCCCCA CCATCCTGAA GCAGCTGACT 1080 TGAAAGAAGG GCAGTAGAGT CTTTTGAAGT TGCAATTACA ATGCCAGCTA GGTGACAATA 1140 CTTTGTAGGG CTGGGTCAGG GGTCTTCAAA AGGCTCTATG TACTCTGTAT CAGCATCCAA 1200 TATATGGTGC TGGTTTCTCC CGTAGCCAGG ATTCACGGGT CCAGGAATCA AGGGGAGGAA 1260 ATGGGAGTGG CACTGCGCAT CATATCCCCT AGGGACCCGC TAGCGAAATT GTTGCTTCCT 1320 GTTCCTGTGA CTTTATGCTC TGCTGGCCTG GAGGTCTTGG TTCCAGAGAG AGGAATGCTC 1380 CTACCAGGAG ACACAACAGT GATTCCATTG AACGGGGGGT AAGGCTGCCA CCTGGCTTCT 1440 TTGGGCTCCC TGTGCCTCTG GGTCAGCAGG CTGAGAGGGG AGTGATGGTG TTGGCTGTGG 1500 AGATTGATCT GGACTACCAA GGGGAAATTG ATCTGGACTG CTCCACAATG AGGCAAGGAA 1560 GAGTGTGTCT GGAGTACAGG ATACTCCTTA GGGCATCTGT TAGTATTACC ATGCCCTGTG 1620 ATTAAGTCAA TGGGAAATTA CAAGGATACA ATCCAGGCAG GACTGTGAAT GACTCAGACC 1680 CTTCAGGAAT GAATGTTTGG GTCACTCTGC CACTTAAAGA ACCACAGCCA GCTGAGGTGC 1740 TTGTTGCAGA CGAAAGGAAC ACAGAACAGG ACAGAGGGAG GTAGTTATAA TAAATACCAG 1800 CTCCAACCAC GTGACCAGTT ACAGAAACAA GGGCCAGAAT 1840
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