| Tag | Content |
|---|
EnhancerAtlas ID | HS098-21604 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:30632990-30635150 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr16:30635107-30635128 | GGTCAGTTTCAGTTTCTCTGC | + | 6.54 | | IRF9 | MA0653.1 | chr16:30635111-30635126 | AGTTTCAGTTTCTCT | - | 6.28 | | SOX10 | MA0442.2 | chr16:30634545-30634556 | TTCTTTGTTTT | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCTCCCATAT CCATAAGCCC ATAGAACTTT TTTCCTTTAA TTTGCACTGT ACAGGTGGGT 60
CGATTAGAAG CTATCGTTTG GGGTAAATTT CCCTTCTGGT TGTACTCCCA AATCCTTGAT 120
TCCCTCATTT CTCCTTATGT GGAGAAGGGT AATTTGCAGG CAATAGGCAG TAGTTGTATA 180
TTCTCCTGGT TCAAAAACCC ACAGATCTTG TGACATTACC ACTACTTGAA TTTCTCCTTC 240
ATGATCAGAG TCAATTCCTG GGACTATAGT AATGCCCTGT AAGTTGAGAC GGCTTCTACC 300
CAAAATTAAT CCCATATATC CTGTTGGCAA AGGACTCCAA ATGCCAGTGG GAATTTTAGT 360
GGTTTTTGTC TCCTCTGACT AACGTAACCC ATTCTCTGAC TGGGAGAGCT ATTCCTGCGC 420
TTCCAGGTGT TCCTGGGGAG AGGGAATCAA TGTTCCTCCG GAGATCCACC CCTGAAGTCG 480
GGTTGTGGCC TGGATGGGGA ATGCCCTCAT TGTTTGAGGG GCCTGGGTCC AGGCCCCCTT 540
CTCATTTCCC AATGTGGGCG GTCCCATTCT GATGAAATTG TGAATGGCAT TGATTAGCCC 600
AATGATTTCC TTTATTGCAA TGAGGGCAAA GTCCTGGCGT TTTTTTCTGT TGGGGGTAGG 660
GTACTGCATT ATAAGATCCC TTCTGCCCAG AGGTCTGATG GCACTCCTTT TTGAAACGTC 720
TGATTTTTCC ACAATTATAA CATTTTCCCC TTTTAGAGTT TGACCCTTGG CCCTTTCTAG 780
ATTTGGCCAC TAATAAATTA GCCGTTGCTT GAGCTAACAT TGTAGAGCGA TGAAGCTCAG 840
TTCCCACATT TTGACAGGCT TTGAGAAAAT TTCCTAAGTT TTTTGTACAT CTTACAGAAG 900
CCAGTGCACG TTTACAATCC TCATTTGCAT TCTCAAAAGC TAAAGTTAAA GTTAGCATCT 960
CTGCAGCCGC GGTATGAGGA ATCTGACACC TCACTGCCTC TAGTAATCAT GCAAGAAAAT 1020
GTGCAGAGGG CTCCTGCAAC CCTTGCATGG CACGTAAAAA AGATTGTATT GGGACCCCCT 1080
TCCTCTGGAA TTGTGGCCAA CGTGTGTTTA GCGGCCAGTG CACACTGCTG ATAAGCAGCT 1140
TCTGGGAGTG CCATTTGATG TTGCAGGTCT GAATAAGGGC CATTACCCAA CAGCATATCC 1200
TCTGTAATGT CCCTGTGTCC AGCAGCACGA TTCTGTCTAG CCTGGTCTGC ACACAGTTCT 1260
TGCCAATTTA AATTCCATGT CAGGTATGAA CTAGCAGACA AACAAGTGCA GGCCAAATGC 1320
TTTACATCAA AGGGTGGAAG GCGCATAGCA CCAAATACAG ATTCTAGCAA TCCTAAAGTA 1380
AATGGGCTCT GTACTCCATT ATTCAGTACA TGAGCTTTTA ATTCCTTCAA CAACTTAAAC 1440
TCTAGTGGGG TGTGTTCATG AATAAACTGC TGTGGATTAT TTGGATCCAG CCTTATAGAA 1500
ATAGGAAAAG CACAAGGTTC GAAGGGCTCT CCAGCTATGG CAGCAGAGCG TAGAATTCTT 1560
TGTTTTGGGG TCTCTATTTC TGTTACTGAA GGAGACAGTA CACGTGTGTC CACTACTGGA 1620
GGGGGCGGTA CAGGCCAATT TTCATCCTCC CTCTCCTGTT TATTATTTCA ATGGGCGCTG 1680
TTGGAGGGAC AAAAGATTCT TTTGAAATTT GAGATTCAGA ACATGGCTCC TGCTGTCCGG 1740
CAGAATAAGA AGGAGACAAT GGCAGGAGGA CAGTATGGAA TAAAGTCAAA ACAGAAGGAT 1800
CAACTTTAAG ACCTTTTTGA TAAGCCTGTT TTAATCCTTC CCCTACACTG TCCCAATTTT 1860
CCGCATCGAG ATGCCTGTCT GTGGAAACCA TGGGTTATGC ATAACAACCT CCTGCAGCAG 1920
CTTAGTGTTT GAGAACTAAC CTGAGCACCA GATTGTTTAA GTAAAACTTT AAGCAACTGC 1980
ACATAATGTT GCTCCTCAGT TGACAAATTC TGCCCCACGT TACCCTGATT CACAAACTTC 2040
CCACTCCCAG TATCTCTTTA GGGCACTGAC CTTATATCCT CTGCCAGCAG ATTTGTCCTG 2100
GGGTTTCTCA CTCATCTGGT CAGTTTCAGT TTCTCTGCTC CAGCAGATCT TCTTCCTTCA 2160
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