| Tag | Content |
|---|
EnhancerAtlas ID | HS108-43134 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chrX:154285210-154286620 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chrX:154285799-154285818 | CATCGCCCCCTTGTGGCGG | - | 6.55 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chrX | 154286198 | 154286248 | | chrX | 154285510 | 154285753 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH0XI155056 | chrX | 154284937 | 154286370 |
| Enhancer Sequence | GAATTAAGAT CTGTAGGTAG GTCCCTCCTG AAGTTTTTTC CCAGCTGGCT GCCTCTACGA 60
CTGTGAGGGT CATGGTTGAG GTCAGTATTG CAGGTTGGCC TCATCCTGCT AGTATGAGAA 120
CGGCTGTGAG TTCTGCCCAC GGTGTGAGGC CACTGTGACC ACTTGGGATT GTGCAGAGCT 180
GGCATGGAGG TTGAACACGC ACAGCTGCAC ACCTTGTTTT CAGTTTAGCT GAACCATCGG 240
TGAAGGAGGC TCAGGCATTT GGGGTTACCT GTGAATCAAG GCCCTATTGT GCCAGCAGTT 300
TTGTTTCAGG TGGTGAAGTG GGAGTTAAGG TTTCCCCCAA AAGAACAGCT GCCACTCCTC 360
CATGCAAAAC CGAGATGATT CAAGGACCAG GCAGCTCCAC CTTTCAGTGC ACTACTTTCA 420
TTTGACTGGA GAGGCCTGCT TAGCTAGGCA CGTATTTTCT CCAGTAGCAG AGTCCAATGA 480
CGCTCTGGAC TTCCTAATTA GTGGTGGTGG GGCGGAAGTT TTTCCTTGGG AAGAGCGTTG 540
TCGCTGTATA TGGTCCGCAG AAACTTGACT TGGAATGTGT TCGGGGTTTC ATCGCCCCCT 600
TGTGGCGGCG ACGTGGTAAC ACCGCACTCA AGGCTTCCAA CTTGTCAACC AATAGGATGG 660
CATCTACGTA GTGAAGGCTT CCCTTCCCTT GTCCTGCAGC GTGCTGGACA GTGTCCCGGC 720
TCAGGGACCC CTTCTGTCCC CTTCCTGGCT ACTATGGGTC GGCCCTGCGT CCTCACCACT 780
TTGAGCCACC CTTTGACCCA GCGTCTCTCC CGCAATGGGA CCTGGTGGGA TGGGGACTTG 840
GAGCATGCTA CAGGAGAGGT AGAACTTTTG AGTCTCTTCT TCCCAAGGTT CTCCCCAGAG 900
TCGGAGAGCA GAGACGGATC CAGGGGCACT TTCTGGCCGC TGCCTGCTCG GGCTCAACAG 960
ATGGAGTCCA ATGTTTCAGT CTCCCCCAAG AATGTGTATC CTCATTGCTG ACACGGGAGC 1020
TGGGTGCGGG GAGAGATGTG GTGGTGGGGA CCCTTGCCTG AGCAGCCCAT TGTCATGAGT 1080
GTTATTGCCA TTGTGATAAT ATGTTAGCAT GACTCTCCTC CCAAATGGCC GCTTGTTTGT 1140
TGCAATCTCC CGCCACTCAG CCTCCAGACA TTCATTAACA GGACAGTGGG GTTCTTGACT 1200
CCCCTACCAC TGGGGTGACA GTCCTTGCTA CTGGATCTGG GCAGTTACTG TCTCATGGAT 1260
GCTGGCAGAA GACGATTCAA GTTGGCGGAC TAGATTCTAC AAGGAATGAT CTCTTGCATA 1320
ATTCTAGCCA ACATGCTCTT GGGGTGGGTG CTTCTGGTTT TGGAAAGCAA AGTTACTGTG 1380
TAGTTAACAA CTATTGTGGT AAGAATAGTC 1410
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