Tag | Content |
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EnhancerAtlas ID | HS182-00162 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:9362300-9363590 |
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 | TGGATGTCAA CTTGACTAGA TTAAGGAATA CCCAGGTAGA TGGTAAAGCA TTGATTATTC 60 TCTATGCTTC AGTACACACT GAGCCTGTCC CTTTTCTGCT GACAGGGAAG CCCAGTGGTT 120 TGACATTGTG TAGAATGATC GGGCTGCCCC AGATGTGTCT GTGAGGGTGT TTTTGGAGGA 180 CACTGGCAAT TGAGTCACTC AACTGGGTGG GGAGGATCTG CCCTCCATGT GGGCAGGCAC 240 CATCCAGTCA GCCGGGGGCC TGGAAGAAGG GTGAATCCTG GCTCTCTGTC CCGGAGCTGG 300 GATGCTCTTC TCCTGCGCTT GGATGTCAGA ACTCCAGGTT CTCTGGCCTT TGGACTCTGG 360 GACTCGTACG AGTGGTCTCC GGAGTCTTTG ACCTGGGACT GGGAATGACC ACGTTCCCCA 420 CCATCCTGAA GCAGCTGACT TGAAAGAAGG GCAGTAGAGT CTTTTGAAGT TGCAATTACA 480 ATGCCAGCTA GGTGACAATA CTTTGTAGGG CTGGGTCAGG GGTCTTCAAA AGGCTCTATG 540 TACTCTGTAT CAGCATCCAA TATATGGTGC TGGTTTCTCC CGTAGCCAGG ATTCACGGGT 600 CCAGGAATCA AGGGGAGGAA ATGGGAGTGG CACTGCGCAT CATATCCCCT AGGGACCCGC 660 TAGCGAAATT GTTGCTTCCT GTTCCTGTGA CTTTATGCTC TGCTGGCCTG GAGGTCTTGG 720 TTCCAGAGAG AGGAATGCTC CTACCAGGAG ACACAACAGT GATTCCATTG AACGGGGGGT 780 AAGGCTGCCA CCTGGCTTCT TTGGGCTCCC TGTGCCTCTG GGTCAGCAGG CTGAGAGGGG 840 AGTGATGGTG TTGGCTGTGG AGATTGATCT GGACTACCAA GGGGAAATTG ATCTGGACTG 900 CTCCACAATG AGGCAAGGAA GAGTGTGTCT GGAGTACAGG ATACTCCTTA GGGCATCTGT 960 TAGTATTACC ATGCCCTGTG ATTAAGTCAA TGGGAAATTA CAAGGATACA ATCCAGGCAG 1020 GACTGTGAAT GACTCAGACC CTTCAGGAAT GAATGTTTGG GTCACTCTGC CACTTAAAGA 1080 ACCACAGCCA GCTGAGGTGC TTGTTGCAGA CGAAAGGAAC ACAGAACAGG ACAGAGGGAG 1140 GTAGTTATAA TAAATACCAG CTCCAACCAC GTGACCAGTT ACAGAAACAA GGGCCAGAAT 1200 TGCTGGGAGT ATTTCCTCCC TATTTTGTTC AGAATACGGT TGTATGCATT TACATGTATA 1260 TTAGGCAAAT ATCTGTTTTC TTTCCTCTCT 1290
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