Tag | Content |
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EnhancerAtlas ID | HS018-00129 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr1:9362180-9363530 |
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 | GCTAAGTGGA ACTACGGTCT TGTTATTGCC TTTATTTGGA AATTAAGTAT GGTTTAAGAA 60 GATGCCAGTG GGTGCCTATG GGTGCCAGTT GGTAAGGGGT GGACCTGTGA TGATTGATTT 120 TGGATGTCAA CTTGACTAGA TTAAGGAATA CCCAGGTAGA TGGTAAAGCA TTGATTATTC 180 TCTATGCTTC AGTACACACT GAGCCTGTCC CTTTTCTGCT GACAGGGAAG CCCAGTGGTT 240 TGACATTGTG TAGAATGATC GGGCTGCCCC AGATGTGTCT GTGAGGGTGT TTTTGGAGGA 300 CACTGGCAAT TGAGTCACTC AACTGGGTGG GGAGGATCTG CCCTCCATGT GGGCAGGCAC 360 CATCCAGTCA GCCGGGGGCC TGGAAGAAGG GTGAATCCTG GCTCTCTGTC CCGGAGCTGG 420 GATGCTCTTC TCCTGCGCTT GGATGTCAGA ACTCCAGGTT CTCTGGCCTT TGGACTCTGG 480 GACTCGTACG AGTGGTCTCC GGAGTCTTTG ACCTGGGACT GGGAATGACC ACGTTCCCCA 540 CCATCCTGAA GCAGCTGACT TGAAAGAAGG GCAGTAGAGT CTTTTGAAGT TGCAATTACA 600 ATGCCAGCTA GGTGACAATA CTTTGTAGGG CTGGGTCAGG GGTCTTCAAA AGGCTCTATG 660 TACTCTGTAT CAGCATCCAA TATATGGTGC TGGTTTCTCC CGTAGCCAGG ATTCACGGGT 720 CCAGGAATCA AGGGGAGGAA ATGGGAGTGG CACTGCGCAT CATATCCCCT AGGGACCCGC 780 TAGCGAAATT GTTGCTTCCT GTTCCTGTGA CTTTATGCTC TGCTGGCCTG GAGGTCTTGG 840 TTCCAGAGAG AGGAATGCTC CTACCAGGAG ACACAACAGT GATTCCATTG AACGGGGGGT 900 AAGGCTGCCA CCTGGCTTCT TTGGGCTCCC TGTGCCTCTG GGTCAGCAGG CTGAGAGGGG 960 AGTGATGGTG TTGGCTGTGG AGATTGATCT GGACTACCAA GGGGAAATTG ATCTGGACTG 1020 CTCCACAATG AGGCAAGGAA GAGTGTGTCT GGAGTACAGG ATACTCCTTA GGGCATCTGT 1080 TAGTATTACC ATGCCCTGTG ATTAAGTCAA TGGGAAATTA CAAGGATACA ATCCAGGCAG 1140 GACTGTGAAT GACTCAGACC CTTCAGGAAT GAATGTTTGG GTCACTCTGC CACTTAAAGA 1200 ACCACAGCCA GCTGAGGTGC TTGTTGCAGA CGAAAGGAAC ACAGAACAGG ACAGAGGGAG 1260 GTAGTTATAA TAAATACCAG CTCCAACCAC GTGACCAGTT ACAGAAACAA GGGCCAGAAT 1320 TGCTGGGAGT ATTTCCTCCC TATTTTGTTC 1350
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