| Tag | Content |
|---|
EnhancerAtlas ID | HS092-05485 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr10:3861690-3863520 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr10:3861862-3861875 | GAACATTCTAGAA | - | 7.34 |
|
| | 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 |
| GH10I003820 | chr10 | 3862626 | 3863206 |
|
Enhancer Sequence | GGAGGGAGAC TCCATCTCAA AAAATAAAAA CAACAGACTC CACTGCTCAG CAAGAGAATG 60
AAGATTAATG GAAATTACAA TGGTTAGGGA AATAGCCATC AACCATCAAT TCGGATCACT 120
CTTTCATGCT CTCAGGGGTA TACCCCATCT CATTCCAAAT AGCCCCGCCT AGGAACATTC 180
TAGAATACTG GCACATCCTT ATCTCACGTC ATGGCTTCCT AACATCTTCA CAGGGAGCGC 240
CTATGCTCCT TTTGGAGTGA AGCGGGCTTT CCAGCACATT TATCTCCAGG ATAAACGTAA 300
TCTAGAGCTC ATTACGACCC CTTAGCAATA TTGACTGCAT ATTTTGAAGC TAAATTTGTG 360
GAGTATCATA GGGCCTGGCT GGGCTGGTTA TCTCTGGCAG GCCTACCGCA TGGAGGCCTG 420
ATGGAAGGGT TCAAAAAAAG ATTTCAATCA GACTTAAGGC AAACACTTCA ATTCACTCCA 480
TACTGGTGAA CACTCTGCCC TCACGCTCAT TGGAAGGCTG CTTGGATCTA TCACTATTAC 540
TTCCTAATTG ACTGGAATCT ATTGAACTTG CAGCTTTGTT GACAGTGCAC TAAGAAGTAC 600
TATTAATCAC AACTACCTCC ATTGGTGAAC GCCATTTATC TCTGTCATCG TGCGTGCTTA 660
AGAAACATCT TTGCACTGAG ATGATCCCAG GTCCAATCAC AATGATCATT ATCTGATGTC 720
ACCTTCAAAA CGTGGCTCAG CCAGAGCAAA ATCTGTAAGG ACAACACCAT GGTGACCAGT 780
GGTCCAACCC ACTATGGGGG AAGTAGAGAG TTGGACAAAA ATGGTTTTGA GCTTTCAGAG 840
GTGACAGGAG TCAAGTAAGT GAGTTTATGA TGTAAGCACA CTTGAATGCT CCTTTAATCT 900
TTAGAGCGGG GGCCACTGAT CTTTGTTAAT TTCCACAAAA TCTCTGCAAA GCCGCGTTCT 960
TCCTGGATTA CTCAGAAAAG CCTTCCAGAT GGTGACGGCC GGGCATCAGA GGCCACACCT 1020
TCAACTGGAG CTCCAACCCC ACAGCGTCAG CACCTTTCTG TCGGGGAGAG AGTGTGACCG 1080
TGATGAGAAC AACAGTGCTT CCACACGGTC TTCCCTTGCA GAAGGAGAAC GTCAGACAGA 1140
GTTCTAGTTA TACCTCGACA TAGCTTTTCA GCTGAAAAAT TCCATTTTAC CAGCTGAGCA 1200
TGTGGCTTGG TCTGGGATAT TTGGTCGCAA AACAAAACAA AACAAAACCT GCTCAAATCG 1260
TGTTAAAACA AGCAAACAAA CTCGCTGAGA AGTTTATATT GGAAGATGCT GAATGTAAGG 1320
GCAGAAAGCA ATGCTATCCC CAGAAGAGAT CAGCGCCTGA GCCTGAGAAG TCATCCAGAG 1380
GGAGGCAGGG CCCTTCCTCA GATCCCACGG GGTCTGGGAT CCTGCTGTCC TCTGCCTCCA 1440
TGGGCAAAGA CCACGATTTC TGTGACATGC CCCATCCAGG ATCCCAGCTA GTGCTGATGA 1500
GGAAGGTCCC CTCGTGGAAT AGTTACTAGT AAATTCATTG AGAGGAGCCC TGGCTTTATT 1560
CCATCCAGGT GTGTGCATGT GTGTACACGC ATGCCTATGT GTATGTGTAC ATAAACACAC 1620
ATATGCGTAC ACTGGGCTTC CAGATTAGAA TGTATTTTAT TGCTGACGTT TATTTGACCA 1680
TGATGCTCTG CCACTGTAAT CAGGTTATTT TCTTGAGTGA GGCTCCAGTC TCTCCACGCA 1740
AATGGAAATA AAAGCAGCAC CTTTCCTGCT GTGAGCCCAC AAACCTCCTT CCACCCTCCG 1800
TCAGGCCGTG CAGAAGGCCG CCATCATTAT 1830
|
