| Tag | Content |
|---|
EnhancerAtlas ID | HS176-13022 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr14:90377080-90378320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr14:90377329-90377344 | TTTTAATAATTAACA | + | 6.05 | | HNF1B | MA0153.2 | chr14:90377330-90377343 | TTTAATAATTAAC | - | 6.14 | | ZNF263 | MA0528.1 | chr14:90377153-90377174 | AGAGGAGGGAGAACGAAAAGA | + | 6 |
|
| | 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 |
| GH14I089909 | chr14 | 90375973 | 90380050 |
|
Enhancer Sequence | GTTGCCAGCT TCACTCGGAA GACAGGAGAG TCGGACGGGT TTTTATATTG TGGGAAGAAG 60
CAGGAAGAAT GGCAGAGGAG GGAGAACGAA AAGATTCAGA AAAGTTAAGC TACTTCTATC 120
TCTTTAGAAT TAACATGAGC CTAATGATTG GAGGACAGGG TAAAAAAACA AAGAGCTAAA 180
TAAAGAGAAC TGGAGACAAT GTAGTATAAT ATTCGGATGT ACAAAGTACA AACCATAAAG 240
TCTATTTTGT TTTAATAATT AACAAAGGTG CACCTAGTAC ACACACTATG GATCAGGCTT 300
GGAGAAAACA GACAAATGAA TCCAAGACTA CTCATTTTGT GAGAGCTTAA AGCAAACAAC 360
TTTTAGCAGT ATTTTAAAGC AAGCTAGTAA AATAAATAGA AGTGAAGTCC AAGGGATTTA 420
AACATGAAAA TTTGGGGAAA AAAGAACTTC GCAAAGCAAA ACAGACAAAA TACAAGGCTA 480
ACCAAACAAA GGCTAAATCA AATAAATAGG CATTGCCGTG TGCCCTGGAG AACTGCCAAG 540
GAGAGTGAAT TTCAACAAAG AATGCTTCTG CCACCAGTTA GGAAAACTTC AATTCCAGAA 600
AGGCTGAAGG AATGCTGCAG GCACTGCCGA GTGACAAGGG GGGTTTGGGG GTGGAGAGGC 660
AGTAGGTCAG ACGTTATTTC AGACTACGCA GACAAACACG AGAACCTTCC TCAAGACAAG 720
TAAAGGCAGC CCACTCCCTC CCAACGTGCT CCGCACACAG CTCCTTGTAA GAAACAAATC 780
CAGGTCAAAG ATGAGAAATT TGCATCTTCA AGGACTGCCT GTAGCAGCCT TCTCTTCTCA 840
ATTTGCAGAT AAAAAGACCC CTGTAAATAC TTCTCAGCCA CCATCCTAGT ATCCACAGTC 900
TTGAGATGAA ACAAGTCCAT GTAGCCCAAG CACAACAAAG CACCAGCAAT CATTGTGTGA 960
GCCTGGATGC TGGGAACAGA GTCCTGCGGC TTTGGGGCTA GAATTGCTGT AGATCAACCA 1020
AGTATTATTC TCTAGGTCAG AGCACAGTTC TCCATTCAGT TGTGGCCTGT AGTAGTCATG 1080
GCAATAGAAA CCACCACTGC CACGGCAGCA GTCCCCACTG ACAGAGCACG TGTCCTGTGC 1140
CAGGCACAGG GCTGAGCAAT TTGCATGAAT TATCCCTGTT AAGCCTCCTA ACAACCTGTC 1200
ATTATCTTAA TTTTATAGCT GTTCCCTCTA CAGATGGGGA 1240
|
