Tag | Content |
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EnhancerAtlas ID | HS050-00448 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:9362310-9363600 |
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 | CTTGACTAGA TTAAGGAATA CCCAGGTAGA TGGTAAAGCA TTGATTATTC TCTATGCTTC 60 AGTACACACT GAGCCTGTCC CTTTTCTGCT GACAGGGAAG CCCAGTGGTT TGACATTGTG 120 TAGAATGATC GGGCTGCCCC AGATGTGTCT GTGAGGGTGT TTTTGGAGGA CACTGGCAAT 180 TGAGTCACTC AACTGGGTGG GGAGGATCTG CCCTCCATGT GGGCAGGCAC CATCCAGTCA 240 GCCGGGGGCC TGGAAGAAGG GTGAATCCTG GCTCTCTGTC CCGGAGCTGG GATGCTCTTC 300 TCCTGCGCTT GGATGTCAGA ACTCCAGGTT CTCTGGCCTT TGGACTCTGG GACTCGTACG 360 AGTGGTCTCC GGAGTCTTTG ACCTGGGACT GGGAATGACC ACGTTCCCCA CCATCCTGAA 420 GCAGCTGACT TGAAAGAAGG GCAGTAGAGT CTTTTGAAGT TGCAATTACA ATGCCAGCTA 480 GGTGACAATA CTTTGTAGGG CTGGGTCAGG GGTCTTCAAA AGGCTCTATG TACTCTGTAT 540 CAGCATCCAA TATATGGTGC TGGTTTCTCC CGTAGCCAGG ATTCACGGGT CCAGGAATCA 600 AGGGGAGGAA ATGGGAGTGG CACTGCGCAT CATATCCCCT AGGGACCCGC TAGCGAAATT 660 GTTGCTTCCT GTTCCTGTGA CTTTATGCTC TGCTGGCCTG GAGGTCTTGG TTCCAGAGAG 720 AGGAATGCTC CTACCAGGAG ACACAACAGT GATTCCATTG AACGGGGGGT AAGGCTGCCA 780 CCTGGCTTCT TTGGGCTCCC TGTGCCTCTG GGTCAGCAGG CTGAGAGGGG AGTGATGGTG 840 TTGGCTGTGG AGATTGATCT GGACTACCAA GGGGAAATTG ATCTGGACTG CTCCACAATG 900 AGGCAAGGAA GAGTGTGTCT GGAGTACAGG ATACTCCTTA GGGCATCTGT TAGTATTACC 960 ATGCCCTGTG ATTAAGTCAA TGGGAAATTA CAAGGATACA ATCCAGGCAG GACTGTGAAT 1020 GACTCAGACC CTTCAGGAAT GAATGTTTGG GTCACTCTGC CACTTAAAGA ACCACAGCCA 1080 GCTGAGGTGC TTGTTGCAGA CGAAAGGAAC ACAGAACAGG ACAGAGGGAG GTAGTTATAA 1140 TAAATACCAG CTCCAACCAC GTGACCAGTT ACAGAAACAA GGGCCAGAAT TGCTGGGAGT 1200 ATTTCCTCCC TATTTTGTTC AGAATACGGT TGTATGCATT TACATGTATA TTAGGCAAAT 1260 ATCTGTTTTC TTTCCTCTCT TACTCCTTAT 1290
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