Tag | Content |
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EnhancerAtlas ID | HS182-07391 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr15:70090630-70091990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr15:70091589-70091600 | GTTTTATTGGG | - | 6.62 | ZNF263 | MA0528.1 | chr15:70091224-70091245 | ACATCCTCCTTCTCTTCCTCC | - | 6.26 | ZNF263 | MA0528.1 | chr15:70091227-70091248 | TCCTCCTTCTCTTCCTCCCTT | - | 7.66 |
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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 |
GH15I069798 | chr15 | 70090740 | 70091901 |
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Enhancer Sequence | GTTTCTGAGT AAGGAATTGC CCCAAAGACC CCTTTCATGT GCTTAATCCC CTTCCTAACT 60 CAGACCCCGT GTAACCAGAG ATACATGTTC ATGCATCACC TCTGTCCTCA AGTTTATATC 120 AGTGGCTGCT TCTATCTGGT GAGAAGGTAG AGGGGAGGGG TGGCCTTCTT GTGAGGCTCC 180 ATGCCTCACA AGTGCGGCAG TGTGGAGAGG CTGAGCAGGC TCGGCAGGCC AGCAGCACCC 240 TGGGATGGCA GGCCTGGCAG GGCTGGTGCC ATGGCAGCTG GCTTCAGGCC CACATCTCCA 300 GTGAAGGCCT CAGAAAGCTT CTGAGCCCAC ATGAGGTGAC TGGACTGGCT GCAAGGAGCT 360 GTGTGAGTAG GAATTGGCCA GGAAAAGTGA ACCCCCATTG GGCAAATTCT GGTCCCAGGC 420 CTGGCTGGAT CTTGCTGTGG GTGAAAACTG ACTCTCTGAG TCTGGGCTGC AGAGAGAGAA 480 AGAGAGATCA GTGAGATGGA GCTTCCCCAA AGGCGTGCAT GGCTTCATCA CAGCAAATCC 540 TCAGGACGCC CAGGGAGCGC TCACTTCCCT ACAGCCTTGT TGACACAGAA CATGACATCC 600 TCCTTCTCTT CCTCCCTTTT CATCTTTGCC AAGGCCATAT CATTGTTGTT TTACTTTGCG 660 CTTGTTTGGT TTTTCCTGCA GTTGTAAGTA TTTTTTCCAG GTTTCTTGGC CACTCCTGTG 720 ACTTCTGTGA ATTGCTTGCT CATCGAGACT GACCTTTCTG TGCTTGTTTT TGCTTTCTCT 780 TCCCTGGATG AAGTAGTTCC TGGCTGAATG ATGACTAAGA ATTGGGTGAG AATGTGAGCA 840 TCTTACCTTC CAATGAGGTT CCTAAGATGG AAGGAAATGG GCCAGTCAGC CTGAAATTCT 900 GGGAGTACAT GAGTCCCTAC TCCCTACAGG AAGAGGGGAG GGATAGTTTT CCTTTGAGAG 960 TTTTATTGGG AGATTGAATA ACCACTACAA ACAAGTATCA TTGGCTGAGC CAAATGATTC 1020 TGGTGGTTTT TCTGATGCCT AGATTCCACG AAAGATGGGG AATTTGGAGG CCCAACTCAG 1080 ATACGGCTCA GCTTCTAGAC CTGAGCTCGG ACCTGCCCTA GAATTAGGGT AGGGAGACTC 1140 AGAGTCAGGG AGGCAGAGGA AAAGCAGACT CTCTCTGCTC CTGGAGCAAC TGTGACGACC 1200 CCTCCACCTG GAGCCTGGCA CGCCCCCATC CCAGCTCCAG GCACAGCTGT GGCCCCCTGC 1260 ACATTTGCTG TCCGTTTACC TTTCCCTTGA AGTTTTCCTG TTTCAGAAAC GTGGACCACC 1320 ACAGCTAGAG AGGTCCTTAA AGGTCTCCCG TAGTCAGGAC 1360
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