Tag | Content |
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EnhancerAtlas ID | HS182-22561 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chrX:153205910-153206930 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SRF | MA0083.3 | chrX:153206221-153206237 | TTACCCTATATGGTCT | + | 6.07 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chrX | 153206276 | 153206342 | chrX | 153206025 | 153206273 |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI153941 | chrX | 153206454 | 153208167 |
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Enhancer Sequence | GCCAGCTCCC TGGTGGCCTC CATATGACAT GGTGTCAGAG GTGTGTAAAC CAGAGCAACT 60 CCATCTTAAA CAGGAGCTGG GTCAAATGAG GCTGAGACCT ACTGGGCTGC ATTCCCAGAC 120 GGCTGAGGCA TTCTAAGTCG CAGGATGAGA TATGAGGTCG GCACAAAATA CAGGTCATAA 180 AGACCTTGCT GATAAAACAG GTTGCAGTAA AGGAGCCGGC CAAAACCCAC CAAAACCAAG 240 GTGGCGACAA CAGTGACCTC TGCTCGTCCT CACTTCCAAC AGTTTACAAA TGCCATGGCA 300 ACGTCAGGAA GTTACCCTAT ATGGTCTAAA AAGGGGAGGC ATGAATAATC CACCCCTTGT 360 TTAGCATATC ATCAAGAAAT AAGCATAAAA ATGGGCAACC AGCCGGGTGC GGTGGCTCAC 420 GCCTATAATC CCAGCACTTT GGGAGGCTGA GGCGGGCGGA TCACCTGAGG TCGGGAGTTC 480 GAGACCAGCC TGACCAACAT GGAGAAACCC CGTCTCTACT AAAAATACAA AATTAGCCAG 540 GCATGGTGGC CCATGCCTGT AATCCTAGCT ACTCGGGAGG CTAGGGCAGG AGAATCGCTT 600 GAACCCGGGA AGCAGAGGTT GTGGTGAGCC GAGATGGCGC CATTGCACTC CAGCCTGGGC 660 AGCAAGAGCA AAACTCCACC TCAAAAAAAA AAAAAAAAAA AAAAAAAAAG GCAACCAGCA 720 GCCCTCAGGG CTGCTCTGCC TATGGAGTAA CCATTCTTTT ATTCCTTTAC TTTCTTAATA 780 AACTTGCTTT CACTTTGCAT TGCGGACTCG CCCTGAATTC TTTCTTGGGC AAGATCCAAG 840 AACCCTCCCT CTTCTGGGGT CTGGATCACG ACCCCTTTCC TGTAACACTG GCACAGAAGC 900 TGAGAGCAGG CCTCTAGGTT CCAATCCAGC CCCAGGTTAC CCTCTAGAGA AGCAACCACC 960 TCCCTGGGCA GAAAGCCTTA GAACAGCGTG GGTCACACAT GGCCCTGGGC GCTCTCCCAC 1020
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