| Tag | Content |
|---|
EnhancerAtlas ID | HS098-10744 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:75099340-75100710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:75100030-75100051 | GAAAAAAAAATGAAAATAAAA | - | 6.36 | | Myod1 | MA0499.1 | chr11:75100217-75100230 | TGCAGCTGCTCCT | + | 6.15 | | STAT1 | MA0137.3 | chr11:75099885-75099896 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr11:75099885-75099896 | TTTCTGGGAAA | + | 6.32 | | Zfx | MA0146.2 | chr11:75100642-75100656 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I075385 | chr11 | 75096397 | 75100243 | | GH11I075389 | chr11 | 75100381 | 75100445 |
|
Enhancer Sequence | GTTCTGGGAT TATAGGTGTG AGCCACCGTG CCTGGCCAAG AGTCAAGGTC TGAACTAGAT 60
TGGATGGTTC TAATAGCTTC TCTTTACGAA AGCCCTCAGC ACTCACCCCT AAGTTAAAGC 120
TCTCTCTTCC CTGTCATACC TGGTTCCTGT CCCTCCCTGG TCAGCTTGGC TGCATGCCAG 180
TCCTTGGCTC TTCCCCTCCC CACTTGCCTC CAAGCTAACC AGCTGCCTGT TCACACAGCC 240
TTATTCTGGG TAGGAAGCTG GGAAGTTGGT AGCATTGGCT TGTTAGCCTC TTGTTCCTGT 300
CCTCCAGCTA CTTAAGTGGA GTCACACAGT ATATTCAGAC CCATATGTGT GGATTTCACT 360
AGTCAAATCC TGGGAAGCCA GTCTCCTGCC TGTTGTTTCT GTGGGGCATG CCCACCCCCC 420
GCTATGTATT GTTCTCCATG CTCAGGCCTT TGAATGGAGT TTGAATGGGG TTACCAATGG 480
TGTCCACTTG GCTGGGGGCC AGGTTTGTAA TGGCGGTAGG ATGCGGAGAG CAGCAGCCCC 540
AACCCTTTCT GGGAAACAAA TTGACCACGT TGCTGTAGTT GGTTGTTATG ACCACCAGAG 600
TGCGCAGTAT GCACAGTTTT GGGAGAGCCA GTTAAGAAGG GTGGCATTTT AAACCTAAAA 660
TTAAGTGATA GCAAAGACGG AACTTATGAT GAAAAAAAAA TGAAAATAAA ATTAAACTAG 720
ATAAACCTAC TGCCTCTGGG TATTCCAGCT GTGTTCCCTG TCTTCAACCT GGGCTCAGTA 780
ACAGCGCTTC AAGAAGGGTC CAGCTGGTCT TTCTTACCTG GCTGACCACT GAAACTGCCC 840
TCCCGCTCCT GGCCCTTTTT GGCCCTGGGA AGGCCCTTGC AGCTGCTCCT GGGCCCCATC 900
TCTCTAGAAC AGATGCTGGT CCCATGCCCC TGCATGACGC CTGATGGGGC TGGGACATCC 960
TTGGCCTTTC TGTTCCAGCA GTCTGATCTG TGGCCGACTT CTTCCCACAT TTTTCCTTTG 1020
AAGGAGCTTT CTCTGTCCTC TACGTTGTGG TAGTGTGGTC CTTTTGCCTG TAACGAAATA 1080
GTGCCTGCTC TGTGTAAGAA TGAAAGGCAC TGGTGTCTTG TGGTCTTCCC CTAAGAGCAG 1140
AGATATGAGC CACGTGTTCG TGTTGGGTAG GACTTGTTGA AACTGACTCA CTAAACAAAA 1200
ACACTGAAGA TTAATGTAAA CCTAAATGCC AAATTGTTTG TCTGCATTAA AAGCAATGAC 1260
GGCCGGGCGC GGTGGCTCAC GCCTATAATC CCAGCACTTT GGGAGGCCGA GGCGGGTGGA 1320
TCATGAGGTC AGGAAATCGA GACCATCCTG GCTAACACGG TGAAACCCCG 1370
|
