| Tag | Content |
|---|
EnhancerAtlas ID | HS150-11955 | Organism | Homo sapiens | Tissue/cell | NT2-D1 | Coordinate | chrX:119396320-119397560 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chrX:119396488-119396509 | CCTTCCTCCTCCTCTCCCTCC | - | 6.01 | | ZNF263 | MA0528.1 | chrX:119396485-119396506 | CTCCCTTCCTCCTCCTCTCCC | - | 6.44 | | ZNF263 | MA0528.1 | chrX:119396482-119396503 | ACTCTCCCTTCCTCCTCCTCT | - | 6.47 | | ZNF263 | MA0528.1 | chrX:119396491-119396512 | TCCTCCTCCTCTCCCTCCCTC | - | 9.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAACCTGGAG AGCCCTTAAA GGCAAAACAA CCTGAGGCAG TGGACTCAAG ACAATCTAGA 60
TTCCTTCTTA AAAACTCAAT TTTCCTCCTC CCTCCAAGAA GATACCCTTT GTTAAAAACA 120
TCGGTATAGT GATTTCCTGA TTTTCCATCT TGCACCCTTC AAACTCTCCC TTCCTCCTCC 180
TCTCCCTCCC TCCTGTTCTG TTGCTTTCCT CAACTAAGAA CTCTCTCCTC TTAACCAGAG 240
AGGGGAACAA AGACCCACCA GGGCAAAGAA TCTCTGTGCC TGGGCATATG GCACTCACTG 300
CCTCTCTAAA TCCCACTACA GAGATGACAT GAGAGGCAGC AGGCCAGTTT TAGGTGTTCC 360
CAGCCACAGA AGGGAGAGGC AAGTTTCCTG AAGTGAAGCT AAAGGCAGTT CTGTCCTGAG 420
AGGCATTAAA AGGCTTCTGT GGGCAGCAGC TGCTGTGGGT GGCAGTTGTA CACTTTGATA 480
ATAAAAGGGG GTGGTACAAC GGCCCTTGGG TTTTCACTTC TTAGTTTTGT GTTTGAGAAG 540
TATGGGGGGA GGGGGTCATG ATTCTCACTT CCCTTTGAGG ATGCTGGGAG TCTTAAGGAT 600
AAAGCTGAAG GGTTCCTGGC AGAGCTAGGG AGCTAACTGG CTGCAGTCCA CACACCCTTG 660
GGGTTTAGCG GGGGAAAAGG CCCATAGTAC CAGTGCATAG TTTCCTAGCA ACAGGCAGGC 720
ACCTTGGGAA AGATCTGGCT TTGTCGCAGC CAGGGAGTTG GCCTGGTGTA TTCTGGTTCC 780
TGCCTGAGAG TGTGACTTTA ATAATGCTGT GGGCAGCTCA GGAGAACAGA ACTTTGAATC 840
CTTGTGCACC ACCAAGCACG AAGAGCATCT AAATAGCCTA CTGCTGGGCC TAGTCAGCTC 900
CAGCTTCCTG AGCGGCTTCT TAGAGGCTGG GGTGGCCAAC AGGCTGATGG TGCTTGAAGA 960
GGAGCACCAC CCTTTCAGGG ACACAGATGG CTTTCCTCTT CCACCTTAGC CTGCCTCCTG 1020
CCTGCCTGAT GGCTGACCCA CACCCTTCAA GATCAATGCG CATTTCCGTC AGGGCATGCT 1080
TCTCTCCAGG AGCCTTGTGG GACAGTGACT TCACAAAGAG CCCAGGAACT GGCTGGTGAT 1140
AATTACTAGT TAAAGACACT GTGTCCCAAG GGTAAAATCC CAGCATCTGT CGGTATTGTG 1200
CATTCCCTCT CTGTTCTGCC CCTGGAAGCA AAGGCTAGGG 1240
|
| |
|
|
|
