| Tag | Content |
|---|
EnhancerAtlas ID | HS073-14635 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr9:116178180-116179800 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Twist2 | MA0633.1 | chr9:116179401-116179411 | ACCATATGTT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 116179294 | 116179374 | | chr9 | 116178213 | 116179300 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I113415 | chr9 | 116178199 | 116179450 |
|
Enhancer Sequence | GGTGTGACTA TTTTCATGTT CTCTAGGACT TTAACTCTGG TTAGACAGCG GTGTTTCTCA 60
GTCAGGACCT ATGATATGCT TCATATTCAT ACCCAGGGAC ACACTCCGCC CCTGCCATGC 120
CCGCCATGTA TAGCGCAGAG CTGTGAGAGA GCTGCCTCCT CTAGTCATTT CCCTGTTTAC 180
ACGCCTTCTT CCTTCAGTGT GTCTTGCTTT CTGCTTCACA CTCTCTGTCG GAGACCAGTC 240
CTTCATGACA TGGTGGGTTT TTGCAGTGGC TTCTGAACTG GTTTCCCTGC CTTTTCTCCT 300
CGAAGCTATT TTACATATGG CCAACAGATT AATCTTCCAA AAATATTGCT TTGTTCATTT 360
CCTTGCTTGA AAAGCCCCTT TATCAGAACT TTGTTTACTA GAGAACAGAC TCAAACCTCC 420
CAACTCTAGA CTGGTGGCCT CTCTCTTTAC TGTCTGGCTC CTCTAATCAG AGTCTTCTCT 480
TCTTGAACAC CAACTTTTCC TCTGTGTGAG ACTGGTTTTC TGATTGTGCT TTTCTGTCAT 540
GCAGTTTCCT AAACCTTAAA GGCCCTCTTC CTTCCTGTCA CTTCATTAAG TCCCTTTCCT 600
GGCCTGTAAG GCCCTACGAG ATCTGGCCTT CCTACTGGAC CTCATCTCGC ATTTCTCCCT 660
TCCTTGTTGA GTAGGCTGCA GCTGCACTGC TCTTTCAATT CCTCATCTAT GCCACACCTC 720
CCACCCCAGG GCTAATGGCC CTACTGTTTC TTCTGAGTAG AACACTTTTT CTCTTAACTA 780
GGTTTTTTTT TTTGTTCTTT TGTTTTTTGT TTTTAAAACA CTATTGACAT TTTGGACCAG 840
ATAATTCTTT GTCCTTTGGG GCTGTCTTAT TTTAGCTACT TCCCTGGCCT GTACCCATTG 900
AATACTAATA GTACCCTACC TCCAGTTATG ACAACCAGAA ATGCCTCCAG ACATTACCAG 960
ATGTCCCCTC GGGGCAAAAT TGCCCCCTTG TTGAGAAATA CTGCCCTAGA TCCTTCCATC 1020
TAATTCCTTT TGGTCATTTG AGTTTAAGCT TAAATGTTGC TTTTTCACAG AAGTCTTCCT 1080
CAACCAGTCT ATTTAAAATT TCCTTACACC CTCATTGTCA TTTAACCAAG CATCATTTTT 1140
CTTCAGTTCT TCTGACCTGA AATGATTTTT TTGATTTGTT TGCCGCCTCT CATGAGAATG 1200
TCAGTCCCTA CAAGAGCAGG GACCATATGT TTCTTTTGTT GGCTGCTCTG TCTCCTATGT 1260
CTTCAACAAT GCATGGCAAG TAGTGGAAAC ATAATAAGTA TTTGTTGATT GAGAGAATAT 1320
GGTCCTTTTC TTCTGTCAAG GTTGAGTTTC CTCATTTCCC ACTAGCCTCT GATACTCTCT 1380
CTTCCAAACT ACCCCCAGTA CTTCAGTCCC TGACATGCTT ATTGATATTT TTATGTTTAT 1440
CTCCTGTTTG TCCAACTGGA TTTTAGGCCC TTTGAAAGCA GGGACCATGA CATTTGTTTA 1500
GTCATTCAAT TCACAACTGT ATTTTAGTGC GGGCCACTGT GATGAATGCT GGGATACAAT 1560
AGTAAACAAC ATACAGTCTT TATCCTCAAG GGACTTTCAG CCTAGTTGGG GAGGCAAAGA 1620
|
