| Tag | Content |
|---|
EnhancerAtlas ID | HS098-58451 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:120441150-120442600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr9:120442160-120442181 | GTTTGGTTTCACTTTCAAGAG | + | 6.02 | | IRF2 | MA0051.1 | chr9:120442159-120442177 | TGTTTGGTTTCACTTTCA | - | 7.1 |
|
| | 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 |
| GH09I117678 | chr9 | 120440558 | 120442278 |
|
Enhancer Sequence | AGGGATCTAT TCATCATATT CCCTTTCTAT TTGGAATACT AAAGGAGAAT TTGTTTGGAA 60
AAAGAATACC TTTCCAACTC CCTATTGTCA TAGTTTGGGA TTAAAGCCAG TACGGTCTGT 120
TCTTTATGAA TGTGTCTAAT CATAAAAGTA TCCCAGAATC TGAGAATGTT TGCACTAGCA 180
GCCCTTGATG ACCAACCTGA GACAATGAGG TGAGAGAGTT TATGTTACTT TCTCAAGTTC 240
ACTGTTAGTG GGTAACCTGG CAGGGACAAA TGACTCAGAT CTTTTTATGC TAAGTCCAGG 300
GTTCAGTTTA TATGGTTTTG TCTCTCAACT GCTTATCTTT GAGAAGAATT AGCTTATGTT 360
ATTGTTTTCC TTGTCAGCAG AATGGAAGCA TTGGATTAGA TCAGTGGCTT TGCCGAGATT 420
TTCCCTTCCA CTTGGTTACT AAGATCCACT TCTTTAGAAT CATTCTTCAT AGGAAAAAAA 480
TGTTTCTTCT CCATTTTTGA TTACTTTGTG CAGCAATTTC AAAGACTTAC CAATCAAAGA 540
AATCAAGGAA GGTATTGGAT AGGAAAACTT TTGAGGGTTC CACATATAGC AGTTTCAACA 600
ATAATCAGAT GTATTTCCTA CTGGTCCTTT TTGCATTCAA GAATGATTAT TTTTCTGAAA 660
GAAAAAATTT GTTCTGAAAT TTCTCAGAGA GCTGAGCTTT GGAAGGCATT CCATTTAGGA 720
AGATGGAGTC ATATCCTTCC TGTTGCATTT AGATAAATGT GGCTAATAGA CAACTTTTTA 780
ACACATGCTT TCTGGCACGT AAATCAGCAC TTCCAGGTTT GAATCTCAGG GATTCGTACT 840
TTCAATTGTT GCCAAATATT CAACATTTGG CTCTCTTGAT CTTTAGTATT AAACTTTTTT 900
TGACTCCATC TTCTTTCTTT CAGCCACTGT TTTCATTATC TAAAAACAGA CACTTAAAGA 960
AATTAGTGAT AATCAGTCTT TTCATAAAGC TGAAAAAGGC CTGAGATATT GTTTGGTTTC 1020
ACTTTCAAGA GTGGTTAAAT AACTGCTCAA GACTTCCATA TGAATAATTT CTCCATTTGC 1080
AAGTTTTTAT CTTTAACTTC TTCTTGGTTT TCTCAATGCC ACAAAACCTT CTTAGTGACA 1140
GGTATTGGGA AAGACAAACT CTTTAGGCCT TCCTTCTTCC TTTGAGGACC AAAGACCATT 1200
TCACTTTTAA TCATTTTATA TATTGTCTCA ACACTGCCTG CCTCTTTATT AACCACCTCT 1260
GTGAAATCTA TTGCTATTAA TCATCAAACA CATGTCTGAG TATTACTGGC AATTATCTCT 1320
GAATGCTTGT TACCTGTTGG TTTTATTACT TGTTTTCTCC TAGAAGAATA GATTGTTTCA 1380
GGTCCATAAC TCTGTTTTAT GTGTATGCAT TTGTGTGTAT GTTTATATTA TTAAATGTAA 1440
TATACATTAC 1450
|
