| Tag | Content |
|---|
EnhancerAtlas ID | HS080-03599 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr10:3087960-3089550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr10:3088039-3088050 | TGCCTGAGGCT | - | 6.32 | | ZNF263 | MA0528.1 | chr10:3088724-3088745 | TCCTCTTCCACCCGCTCCTCC | - | 7.59 |
|
| | 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 |
| GH10I003044 | chr10 | 3087138 | 3091558 |
|
Enhancer Sequence | ACTGACTAAC TCAGGGGTAC TTGTCATTCC TGGACACTTG GTCCCCAGCC CACCCGGCTC 60
TCCTCTCTAG GAAGCAAGCT GCCTGAGGCT ATTTTAAGTG CTCTCCTTTC TCCACCAAGA 120
ATTGGAATCT GCCCAGCTGA GCCCCAGACG CTGGAGGGGT CCCGGGGGTC AGTCAGCCCT 180
GCACCACCCT CCAGCTCCTC TTCTGGCCAT ACAAGGAAGT CCAGTGTGGG GATGACTAAG 240
CAGCTGACCC GGGGCGGGGG AGGGCAGCCC TGGAGCGGGA GGCAGGGCCG GCCTCTCCTG 300
CCAGCCATCA GCCCCTGCGG GCTTGTCCTG TGGTGAAAAG TCCCAGGCCT CCACCCAGGC 360
AGCACCTGAC CTCTCTGCTC CCTGAGAGGA GTGAAGTGGA CCTCAAGGTC TGGAGGTGGA 420
GGCACAGCCT TGCACTGACA TCAGGCCCTA AGCTCTAGTT CTACACAGAG ATAGCCCATC 480
TGTCCTGGCC TCCCGGGGGC TCCCAGGGGC AGGGAGATCT GGCCTGGCCT TCCCAGCAAT 540
GCGTGCCTCA GTGGAGAAAC CCCAGCTTCC CAGCATTAGG ACACACACTC TCTCTCACAC 600
CCTCCGTGGT TCCCACTGAC CTCACTGCAA AGTCCACAGT AGAAACTCAC AGAGACCTGC 660
TGAAGAGGCA CCTGCCCAGC TGTCAGCCTG TTCCTCCACC TGCTCCCCCA ACCTGCCCTC 720
TCACCTGCTG TCTACACTCA TTCCCCCCAC CTGCTCTCTC ACCTTCCTCT TCCACCCGCT 780
CCTCCCACCT GCTCTCTCAC CTGCTGTCTA CACCTGCTCC CCCCACCTGC TCTCTCACCT 840
GTTGTCTACA CCTGCTCCCC CCACCTGCTC TCTCACCTGC TGTCTACACC TGTTCTCTGC 900
TCTGGCTGCC CCCACCCATC CATCTCCCCC ACACCCTTCT TGGACACTGC CCGGTGCTGC 960
CCAGCTCCCT CACACAACAC TGCCCCTCCC CACTCATGTC CTGCTTCCTC GATGGTCTTC 1020
CCAGAGGAGG CCCCACGTTC TCAGCCCCTA CCTGTTCCTC AGGTCACCAT TTCCTGGAGC 1080
CACCTTCCAT CCCCCAGAAC TCAGCTGGGC CCTGCAGACA TGTACATGCT ACCAGGTGAC 1140
CTGTGGCCAC TCCTCCTGCA AAGCTTTTCC AGGTGTCTCT GTTTTTCTTG TTCCTCAGAA 1200
CGATAAAAGT TCCCAGATCC CAGGGACTTT CAGGCTGCTC CCACCACAGA GCTGGCCAGC 1260
ATCCTTTGAG GCAGAGAGAT GCTAGGGGTA AGTCCATGAG GCGGGGCCTG TCTCCGGGGC 1320
TGGGAACCTG GAGTCACTGA ACCGGGAGGC CAGCGTGTTG CCCAGGGCTT CGCCTTCCTG 1380
CTGTGGTTTG AAAGACAGGA ATACTAATGA GGTTTCCTTA ACCTCCTAAG TGAGTGTGTG 1440
TGTGTATGTG AATGTATGCA CGTGCACACA CTCACACTCA CACACACACA CACCAGCCCC 1500
TGTAAACAAG GCTGCAGGTT CCAGAGAAGA TGGCTCCCTC AACCCACAGA GAATTAAGAC 1560
AAATCCTCAT GAAGCCACGA GCAGAAGTCG 1590
|
