| Tag | Content |
|---|
EnhancerAtlas ID | HS108-42304 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chrX:41112110-41114010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chrX:41113118-41113137 | TGCTGCCCTCTAGAGGCCG | - | 6.91 | | Foxd3 | MA0041.1 | chrX:41113318-41113330 | GTTTGTTTGTTT | + | 6.32 | | HES2 | MA0616.2 | chrX:41113995-41114005 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chrX:41113995-41114005 | GGCACGTGCC | - | 6.02 | | MEF2A | MA0052.3 | chrX:41113862-41113874 | TTTATTTTTAGA | - | 6.07 | | ZNF263 | MA0528.1 | chrX:41112147-41112168 | TCCTTCCTTTCTGCCTCCTCA | - | 6.1 |
|
| | 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 |
| GH0XI041253 | chrX | 41112254 | 41113453 |
|
Enhancer Sequence | AATAGTCAAT TTCATCAGAG TGCTTTTCTC ACCTAGATCC TTCCTTTCTG CCTCCTCACC 60
ACACCCCTTT ACCCACAAAC AGTGGGAGGG GAGCCCTGGA CACTCTCAGC TTCCTCCTGC 120
CCCTGAGTTC CAGCGATCAA AGATAAAATT GAAAACATTA GCTATGCCCA CTGCTCCCTG 180
GTGGAAGGCA GCCACCTTCT GAGGAGGTCC CATGGGAGAG TGAGTCCCCT CCCCGTGCAT 240
AACCCGACCC CCAAATTGGG GGCTCTTCAG ACCTCATCAG ATCCTGCACA GGCCCCCCAG 300
GATAGGTGCT TGGGGTGCAG CAGCTGGCCA AGGCGCTGTG CCTTGTTGTC TAGGTGGTGT 360
GCCCACCCGG GCTCCCGGTC CCGCCTGGTC ACAAGCATCC CCGCGTCAGC TGATGAACAC 420
CCCTGTCCAG CAGGTGCCAG ACACCCGAAA TCAAGAGGAG TGTCCTGTGC TCCAGGAGCC 480
TGAGAGGTGG CAAAGTCCCC GGGGGGAGGC GTGATGGTAG GGAAGGCTTC TGACATACCT 540
CTGCAGGGGC CAGGGCCCTG AGTCCCGGGT CCCCATGGTG TGTTTCTGTG TGAAGTCAGT 600
GGCACTGCCA GCGCCGTGGT CATATTACCT AGGCCACAGC TGCCAGGCCT GCAAGCTCTT 660
TCCTACTTCC CTTAGGTGCC CAGACCCAAA GTCAAGAGGA CCTTGACCCG TGGGGGTCGT 720
GGGGAATGAA AACCGTCCTG CGAACTTGAA CTTCACTAGG GAGGCGGCGC TCTCTCTGCC 780
CCGGTTCTAT CACGCGCATC CGTTAGGAAC TAAGCGGCAC CTGCGCGAGG CTAGGCTTGT 840
TGACATATTT CTTGCTGGCG GCGTCCTCTC GCGTGGAGCA CGACTGCGCA AAGCGCCGAC 900
AGTCCCCCGA GCGAGGACGG CAGCGAGACT CCGAAGCCCC CTTAGCAACC AAGCCGGTGC 960
CGCTGCCCTT GCGCCGGGAC TGCAGCCGGG TCTTCCGAAG TGAGGATATG CTGCCCTCTA 1020
GAGGCCGCGG GGTGACATGG CCCATGAGGC TGTCTGGGCA GGGTGGGTTC GGGTGGGAGG 1080
AACCAAGGTG GACAAGCCTC GAAGTAAGAG ATCTGTTCAA GGTCACAGGG AGTCGGGACT 1140
CATGCGGAGG CACAGATCCA AGCTCTCTGT ACTGGGCCCT TTGGTATTCT GTTGGCTCCT 1200
ATTTTTTTGT TTGTTTGTTT TTTGTTTTTT GTTTTAGATG GAATCTCTGT AGCCCAGGCT 1260
GGAGGGCAGT GGCGCGATCT CGGCTCACCA CAACCTCCAC TGCTGGGATC AAGCGATTCT 1320
CCTGCCTCAG CCTCCCGAGT AGCGGGGATT ACAGGCGTGC GCCACCATGC TGGCTAAATT 1380
TTGTATTTCT TAGCTTTTTT TAAGCTTTTT TTTTTTTTTT TTTTGAGATG GGGTTTCGCT 1440
CTTGTTGCCT AGGCTAAAGT GCAGTGGCGT GATCTTGGCT CACTGCGACC TCCACCTCCA 1500
GGGTTCAAGA GATTCTCCTG CCTCAGCCTC CCGAGTAGCT GGGATTACAG GCGCGTGCCA 1560
CCATGCCTGG CTAATTTTTT GTAGTTTTAC TAGAGATGGG GTTTCACCAT GTTTGGTAGA 1620
GATGGGGTTT CACCATGGTC TCAAACTCCT GACCTCAGGT GATCTGCCCA CCTCGGCTTT 1680
CCAAAGTGTT GGGATTACAG GCATGAGCCA CCGTGCCCTG CTGCCCCTGT TATTTATTTA 1740
TTTATTTATT TATTTATTTT TAGATGGGAT TTCACTCCTG TTGCCCAGGC TGGAGTACAA 1800
TGGTGCGATC TCAGCTCACC GCAACCTCTG CCTCCTGGGT TCAAGCGACT CTCCTGCCTC 1860
AGCCTCCCGA GTAGCTGGGA TTACAGGCAC GTGCCACCAC 1900
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