| Tag | Content |
|---|
EnhancerAtlas ID | HS147-06536 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr10:75872510-75873940 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr10:75873695-75873716 | TTTCCCCCTCCTCTCTCCTCT | - | 6.35 | | ZNF263 | MA0528.1 | chr10:75873688-75873709 | CCTCTCCTTTCCCCCTCCTCT | - | 6.83 |
|
| | 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 |
| GH10I074112 | chr10 | 75872446 | 75874168 |
|
Enhancer Sequence | AATGAACCAA AGCTAGTTTG GAGAGTAGGG TGATTGGGGT GATCACTTTT CCCTTTAAAG 60
GTGGCATGCT GCAAGAAGAA AGGCTTTGAA GAGTGATGGG TAGTCACTAA CCATGGCACT 120
ATGCTATCTT CTAACCAACG TGATGGGGTC CTGGAATGAT CCTAGGTCTG CACTAGAAGA 180
GGTAGACCCA GAGGACCTTG TCTAACATAC CCCTTGCTTC TTGACTTCTT CCCATACCTG 240
CGTTCTCTCC GGCCTCAATT ACTGCCTGAG ATGTTACACC CTTCCAGCAT AAATGATGAA 300
CCGCTTCATG GTGCCTGTAG AGGCCTCTTG CAGAGCACCC TGCAGTGGTA TGGTTTGTGT 360
ATGCCTCACT GCACTGTAGA GAAATGAAGA GCATGAGGGG AAAAATGAGT AGGGCCTGGA 420
CTTTTAGCTA GTTTTGAACA CTGCAGTTGC TATGACTTGG GGTTGTTAGC AGCCAAAAGA 480
GGAGCTTTCA TGAGAGGGCA CAGAATACAT AACTTGTCTG TTTCTTTACT ATGACCCATG 540
AGGGTTTTAG TAAACCAAAA TGCCAAGTCT AAGATAAACT GCCATTCCTT GGAGTGAGGG 600
TTCCATTTAC AGCCTGAATC ACGACTTTTA TTTTCCTAAT GCCTTCTCTT GCATCCTCTT 660
AGCTGAAGGT TCCTTTAACT GGAGTCTTCA CTTAGCTGAG GGGACTGAAG AATTGATTCT 720
TTACCCTTTT ACGTGGGAAA AATTAAAGCA ACATGTTCGT TCAGGCTGAC AGGACAAATA 780
AGAGGCAGTA GAGGGATAGC CAGAGCAGGC TAGATCAGAA AATATCTTTT TTTTTTTTTT 840
CCCTCACCCA GCTGAGAATA GTTACTTGGG TTTGAAATTC TAGTTAAGTA GCAAGAACGC 900
TTGGCTGCTA TTTGCAACAA GGGTAAGCAT GAAGAGGGTG ATTTCAGCAT CTGGAAAGGC 960
TCCTCTGTAT TTTTCCCCTC AGGCCAGCTC TACTGCTTTC TCCCTATAGA AATGAAAGTG 1020
CCTGTTTAAC CAGCTCCTTG GCCCTGTCCC CAGTTTATTG ATATGATTAA CCTGGAGATG 1080
CCAAAGTGCT TGTTCAGTGC TGTGCCTGGG GTGCACATCT TGCCCTTTCA GACTAATATC 1140
TGGGTCTTCC TTTTTTTTAG TCAGGAAATG TCTCTCTCCC TCTCCTTTCC CCCTCCTCTC 1200
TCCTCTCTCT TTGTTTCTCA CACTGAGTGC TTGGGCGAGT GCCCTGTCTC ATTCTTTTTT 1260
TTTCTTCCAG TGCTATCCGT ATCACTCAAG AACGGCCCTT TTCTCCTCTT CTCACCCTTC 1320
CGGAGGGATG CTAAGGTGGC AAGCTCCCTC CTCTTCTCTG TGCTTCTCCT TCCTTCCTTA 1380
ACATGGCCAG AGCGTGGGCA GAGCTCACAC TGTATCTTTG CTTCCCTCTA 1430
|
