Tag | Content |
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EnhancerAtlas ID | HS002-00066 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:9362420-9363600 |
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 | TGACATTGTG TAGAATGATC GGGCTGCCCC AGATGTGTCT GTGAGGGTGT TTTTGGAGGA 60 CACTGGCAAT TGAGTCACTC AACTGGGTGG GGAGGATCTG CCCTCCATGT GGGCAGGCAC 120 CATCCAGTCA GCCGGGGGCC TGGAAGAAGG GTGAATCCTG GCTCTCTGTC CCGGAGCTGG 180 GATGCTCTTC TCCTGCGCTT GGATGTCAGA ACTCCAGGTT CTCTGGCCTT TGGACTCTGG 240 GACTCGTACG AGTGGTCTCC GGAGTCTTTG ACCTGGGACT GGGAATGACC ACGTTCCCCA 300 CCATCCTGAA GCAGCTGACT TGAAAGAAGG GCAGTAGAGT CTTTTGAAGT TGCAATTACA 360 ATGCCAGCTA GGTGACAATA CTTTGTAGGG CTGGGTCAGG GGTCTTCAAA AGGCTCTATG 420 TACTCTGTAT CAGCATCCAA TATATGGTGC TGGTTTCTCC CGTAGCCAGG ATTCACGGGT 480 CCAGGAATCA AGGGGAGGAA ATGGGAGTGG CACTGCGCAT CATATCCCCT AGGGACCCGC 540 TAGCGAAATT GTTGCTTCCT GTTCCTGTGA CTTTATGCTC TGCTGGCCTG GAGGTCTTGG 600 TTCCAGAGAG AGGAATGCTC CTACCAGGAG ACACAACAGT GATTCCATTG AACGGGGGGT 660 AAGGCTGCCA CCTGGCTTCT TTGGGCTCCC TGTGCCTCTG GGTCAGCAGG CTGAGAGGGG 720 AGTGATGGTG TTGGCTGTGG AGATTGATCT GGACTACCAA GGGGAAATTG ATCTGGACTG 780 CTCCACAATG AGGCAAGGAA GAGTGTGTCT GGAGTACAGG ATACTCCTTA GGGCATCTGT 840 TAGTATTACC ATGCCCTGTG ATTAAGTCAA TGGGAAATTA CAAGGATACA ATCCAGGCAG 900 GACTGTGAAT GACTCAGACC CTTCAGGAAT GAATGTTTGG GTCACTCTGC CACTTAAAGA 960 ACCACAGCCA GCTGAGGTGC TTGTTGCAGA CGAAAGGAAC ACAGAACAGG ACAGAGGGAG 1020 GTAGTTATAA TAAATACCAG CTCCAACCAC GTGACCAGTT ACAGAAACAA GGGCCAGAAT 1080 TGCTGGGAGT ATTTCCTCCC TATTTTGTTC AGAATACGGT TGTATGCATT TACATGTATA 1140 TTAGGCAAAT ATCTGTTTTC TTTCCTCTCT TACTCCTTAT 1180
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