Tag | Content |
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EnhancerAtlas ID | HS148-16892 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr7:55063260-55064020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr7:55063867-55063881 | ATTGTTTACCTTGG | - | 7.22 | IRF1 | MA0050.2 | chr7:55063988-55064009 | TTCCTCTTTCTCTTTCTCTCC | + | 6.29 | SPI1 | MA0080.4 | chr7:55063985-55063999 | GACTTCCTCTTTCT | - | 6.21 | SPIC | MA0687.1 | chr7:55063985-55063999 | GACTTCCTCTTTCT | - | 6.67 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I054994 | chr7 | 55062600 | 55064548 |
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Enhancer Sequence | AGGTGGAAGG AGGTAACCAA CATTGATTGA GCAACCATCA TGTACCAAGA GCTTTAATTT 60 TCACAATGAT ATAGTAAAAC AGGAGTGATT AGGTCTCACT TCACTGAGGA AGAAACTGAG 120 GTTGAGTAAC TTTCCAGTTT TATGCAATTA GTGGTAAGCT GAGCTGAAGC CTGAGCTTCA 180 CATGCCATGA CTTGGATGGG TAAGCTTCAA TTACTCTCAC TTAAAGGCTA GCTCATGTGT 240 TGTCAGGGAT GCTCAGTGGG CCAGAACCAA TAATTGGGTT CCAAAGGGAA TAATTAAGAT 300 TGGAGCAAAA CCTTGTAGAT TGGGGCTGAG TCAAGTCTGA ACGTCAAAAC AGAGAGACCA 360 GGTTCAAAGA GCAGACGTGG AATCATAAAA ACATAGAATC AAAAGACAAG AGTCCCATAA 420 AAACAGGATC TGAGTCAGTC TTCAGCCCAC TTAAATCTTT CTTCCACCCC CAAACTTTCC 480 CAAAACAGCA CTCACTAAGG TCACTAATGA CTTCAACATA ATCAAATCCA ATGGGTAATA 540 CTTTATCTTT CTCTTCCGTG GCTTCTCAGC AGCATTGGCA TTCTGAGCAC TTCCGCCTTT 600 GTGAATCATT GTTTACCTTG GGCTTCCCCG TCTTCCTTAC CTATCTGTCT GCTTCATCTC 660 AATCTTACTT GCCACTTCAT CCTCCTCCAC CTCAGTCATA AATGTGGTTT CCAAGATCAA 720 TGTGAGACTT CCTCTTTCTC TTTCTCTCCA TCTCTCTCCT 760
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