| Tag | Content |
|---|
EnhancerAtlas ID | HS098-57795 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:94942680-94944310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr9:94943309-94943320 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr9:94943309-94943320 | CTGAGTCACCC | - | 6.02 |
|
| | 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 |
| GH09I092180 | chr9 | 94942341 | 94944165 |
|
Enhancer Sequence | GTGGAAAGTG CCTTCGCTGT CTCAGATCCA CCCCTCAGTG CTTCCCTACT CGGAGTGCCC 60
ACCCAGCTTG TTTGAGGGCA AGAGGAGGCC TGGTCCTCCG GGCAATGGTC CCTGACTACT 120
CCAGGCCTCA GTGATCCATG CAGATGAACC ACCTGCTTGC CAACATCACG CTTGATTCTG 180
GGCCAGTCTG GGAGAGACGG GAAGGACTCC AAGGGTCTCC TGGCCCTGAC CCTTGGGAGC 240
TCCGAGTACG CAGAGGAAGT CCCAACATTA ATGTACCCCA TGCAAACTAG GCTGTGGTTT 300
GCACTACTGT GGAGACAGAG GAAGCCACGT GTAACTGGTG GGCCTGGTGG TGAATTCCAC 360
ATTGGGTGAA AGGGCAGGTC CGAGATAGGC CCAGAAGAAT GAGTACAACT CAGATAGAGG 420
AAAACAGACA AGGCCAGGAA CATGGAAGCC AACACTTATT AAGCACCTGC TAAATGCCAG 480
GCATGGTGCT ACATTTCTAC AGGAACCTTA TGAAGTGGAG GCTGTTAGCA AGCCCACTGC 540
ACGGGTGAGA AAACTTAGCT AAGGTCACAG CACATGCAAG TGACAGAGTG AAGACTGCAA 600
CCAGCTGTGT CCTGCTCGCA GTCTGAGCGC TGAGTCACCC TGCAGCTCTC TCTCTCCTCA 660
AAGCTGTTTT TGCGTGCTCC ATGCAGGGAA GAGAAGAGAG CCACAGGGTG GAGGCGGGGA 720
CCACAGCAGA TGGCTCAGCA GGAGATGAAT CCAGATGGAA TCTCACAGAC AGGCAGTGGT 780
GGCTGAAAGG CTCAGGAGAT GTCCACCTCA GTGGTGTCCT TGGCCTGGGC AAGGAACTAG 840
AGGAGGGGCA GGGCTGAGGG CACTGTGGAA TGTCCAGCAG GTAGGCAAAG TGTGCTGGCC 900
CTGAGGCTCC AGGGGCATGA CCTTTGCAAG AGAGGCTGGT GGGGAACAAG GCTGGAAGGG 960
AGCTGGACTA AGGACTTGTT GGCTGAGCCC CACCAGGGCT GGGCATTGGG CAGGCTCCCT 1020
GCTCCCCCTG GGGTACAGAT GACTCTGTGA GGAGAAGGGG CCAGGCCACA GCCAGAAAGG 1080
AGGAACAATG AAGTATGTGG ACGTGGACAG GAAACCAAGA AGCCTGGGGC TGGCTCCCGC 1140
TGGGCAGGCA GGTGGGCTGA GCTCCCTCCC ACTACTCAGT TAGCTTGCCG GGCAATATTG 1200
AAAACAGTGC TGCCAATGAG CCCTTCCCAC GGGCCAGGGG GACTCAGGGC TCAGACTAGG 1260
GGGAAGGAAA GACCTGGTTC TAGTTTTCAA TCTATCATTT TGCTAGCATT GTGGTCTTTG 1320
CCAAACATAT CCATTTCCAA GGGCTTGCCA TAACACACTG CCACCACCTT GGTGGCTTAG 1380
AAGCAACAGA AATGTATTCT CTCACAGTTC TAGAGGCCAC AAAACTGAAA TCAGTGTGCT 1440
TCCAGGGACA CACTACCTCC AAAGGCTCTA GGGGAAGACC CTCCCTTGGC TGTTCCAGCT 1500
TCTGGCGGCA CAGGCATTCC TTGGCTTGTG GCGGCATCCC TCTCCTCTCC ATGTCTTTCT 1560
GCACATGGCC ATCTTCTCCA TGTGTGTCTC TATGGCCTCT CCCCCTCTTT TAAGGACACC 1620
AGTCATTGAA 1630
|
