| Tag | Content |
|---|
EnhancerAtlas ID | HS138-31185 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr4:149716080-149717210 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr4:149716973-149716994 | CCTACCACTTCATCCTCCTTC | - | 6.23 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH04I148795 | chr4 | 149716381 | 149716631 |
| Enhancer Sequence | TATATTTTAT ATTCTAGAAG TTCTAAAACT TGGAGACAAA GAGATATGTT GGGGTGAGGA 60
AGAATATGGG GGGATATAAT GGATATTTAA TCTTCTAACA AAATGCACAG ACTTCACTCA 120
CTGTGTCTTA CCCTGGGTCA GTGATATCCT AGGAAAAGCT CCTTTTGGTA TCAACGGGAA 180
GTTTTCACAC ATAAAGATTA GGGGGTCGTG TCTCTGAGTA TGAAACACAT GAGGCAGATT 240
CTTAAGCTAA AGCATTCATA CCAGCTGGGA AGAGGGGTTT TCCCGAGGAA CAGTAACTTC 300
CCTCTACATC CAGGAAAGCC TCATGGTGTG GATGGGCGTC CAACAAGCAG GCTGTTCTGG 360
CCCTCTTTGG GTGCTGACTC TGTGTTCCCA AGGGCCATTG ATAAGCTAAG CAGGAATAGT 420
GTAACCACAG GAATGCCTGC TGATAACAGG AAAGTAGGCG GCTGCATTCC TGAGCCATGG 480
CTGATGCTGC TCCATCCACT GCCAAGGTGT AGAAAAAAGA GACAAAGTAG TAAATTCTAA 540
AGATTTGTCA GTCTGGGTTG GCAGCTCTTA GAGAATGGAT ATGTGGCAAA TATGTCTCTC 600
CCTCTGTGTG TGTGTATGTT TGTGTGTGTG CGTGTGCGTG TGTGTGTGTG TGTTAGAGAG 660
AGAGAGAGAG AGAAATCTGT GCCAGAGCTG AGGCACAGAT CCTATCTGTG TATAGAGGTG 720
TGCTACTCTA GTGCCCTGTC TCCAAGCCTT CAGGGAAGAC TACTTGACCA ACTATTACTC 780
CTGCTTCAGA TGTGGAACCT GCTAGAAGCC TGCCTTTACC TTCTAATACT TTGACTCTAG 840
CAGCCTGAGA GCCACACAAT TCAAAATGCA AACTGGGCTC TCCACGATCT CTACCTACCA 900
CTTCATCCTC CTTCCCCGCC ACTTCTCTAA AACCAGCTTT CATGAACACA CACCTGCTTT 960
GCACATGATT TCTCTTCTGC TTGGCAGAAT CCTATGTACC TTTCAAGATC AGCTTAGGAG 1020
TCCCTTTCTC TAGGAAGGAG ATTTTCCCTC CTCCTAGCTC CTCACGGAAA TGATAACTAT 1080
ACCTCTCAGG GTTCCTTTTA TTCCTTAAAC AGTGTCCCTT AACTCATTGG 1130
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