Tag | Content |
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EnhancerAtlas ID | HS108-42826 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chrX:122918170-122919560 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chrX:122919031-122919043 | GCAATCACTGCA | + | 6.14 | NFAT5 | MA0606.1 | chrX:122919331-122919341 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chrX:122919331-122919341 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chrX:122919331-122919341 | AATGGAAAAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29234 | chrX:122918370-122919643 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI123784 | chrX | 122918024 | 122919388 |
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Enhancer Sequence | AAAAAAAAAA AAGTTGGCGG ATGCGGGGAC AGCAAAGGGC TTAAGTAGAC ATTTCTTCAA 60 AGAAGATATA CAAATGGCTG ATAAAGACAT TTAAAGATAT TCAGGGCCAG ACGTGGTGGC 120 CCACATCTAT AATCCCAGCA CTTTGGGCTG CCAACGTGGG AGGATATCTT GAGCCCAGGA 180 GTTCACGACC AGCCTGGGCA ACATAGTGAG ACTATCTCTA CATAAAAACA AAAAATAAGG 240 CTGGGCATGG TTGCTCACAC CTGTAATCCC AGCAATTTGG GAGGCCGAGG CAGGCAGATC 300 ACCTGAGGTC AGGAGTTTGA GACCAGCCTG GCCAACGTGG CAAAACGCTG TCTCTACTAA 360 AAACTACAAA AATTAGCCTG GCATGGTGGC GGGCGCCTGT AATCCCAGCT ACTTGGGAGG 420 CTGAGACAGG AGAATCGCTT GAACTTGGGA GGCCGAGGTT GCAGTGAGCC GAGATTGAGC 480 CATTGCACTC CAGCCTGGGT GACAGAGCAA AACTCCATCT CAAAAATAAA TGACTAAATA 540 AAATAAAGAT GTTCAACATC ACTAATCACT AAGGAAATGC AAACCAAAAC CACGAGATAC 600 CATTTTACAT GCAGAAGAAT GGCTATAATT TTAGAAAGAT AGAGTTTCAC AAGTCTAGAC 660 GCTGAGCCGC AGCACATTTG CAACGTCACG TGGAAGCTGA AACTGCACCT CCCACGTGGC 720 CCCTCTAGCC AGCTGAGAAC CTCAGATAAG AACTACACCC AGGCCAGCAC CAGCAGCTCA 780 GCCACTAGCA GCAGCCCCAC CCTCTGCAGC TGGCTCTCCT GCTGCTGCAC TCCGCGGCAG 840 CCAGGTCTGA TGGCCCGGGC GGCAATCACT GCAGCTGGCA TGGCTGTGGA CTCTGCTGTG 900 GGGCACATAC TGGGTCATGC CATCAGTGGG AGCTTCAGTG GAGTAAATAA TGCTGAGCCC 960 CCAAGTGGTG ACATCACTTA CCAGAAGCCT CAGGGAACCC ACCCGGCACA GCAGCAGTAG 1020 GCTTTCTTGT ATGAGATAAA ATGGTTTTTG GAATGTGCCC AGAATCAGGG AGACATAAAG 1080 TTCTGTGAGG GTTTCCATGA GGTGGTGAAA CAGTGCAGAC TTGCAAATGG ATTTATCTAA 1140 TCAAGAAGTT CAAATTGAAG AAATGGAAAA TCAGCTCTCA CAACTAAGTT AATTTAGCAT 1200 AAAAACATAA TTGATAGCCG GGCGTGGTGG CTCACGCCTG TAATCCCAGC ACTTTGGGAG 1260 GCCGAGGCAG GCGGATCACC TGAGGTGGGG AGTGCGAGAC CAGCCTAACC AACATGGAGA 1320 AACTCCGTCT CTACTAAAAA AAAAAAAAAT ACGAAAAATG AGCCGGGCGT GCTGGCGCAT 1380 GCCTGTAATC 1390
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