Tag | Content |
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EnhancerAtlas ID | HS098-33810 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr2:239860220-239861220 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr2:239860585-239860596 | CATGAGTCACT | - | 6.14 |
| | 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 |
GH02I238937 | chr2 | 239859392 | 239861781 |
| Enhancer Sequence | GTGACTTCCC ACCCGGGTGG CGGCTGAGCT GGGGAGTCCA ACAGCTCCCT TTGCTCAGGC 60 TTCCGCTGTT TTCCTGGGAA TCTAAACCCT GGAGGGCCCA GCAGGTCTGT CAGCCTCTGG 120 TGGGGTGACC CCATGAGGAA GCATGCCTGC CAGATGTCCC TGCCAGCTCT TCCTGCGAAC 180 ACACACCCAG AGCCTGTGCA GGAGTGTCCA CACGCACGCA CGCACACACC CATTAATCAG 240 GGCTCGCCTC TATCATCCCT CTGACCTCCC GCCAAGGCTG CCTTGGTTGA GGCGATTCCC 300 ATTGCATGAG GACCGGGATG CTTTCTGAGG GCTGGGAGGG TTTTCGTCAG TTGGGTTCGG 360 TCCAGCATGA GTCACTGTCC GCCTCTTCTC ATTAATTAGT GTTCTGGGAG TTGCTGGTGT 420 AACTCTGGTG AAGTCTAGAG AAATTAATCA AAGTATATCT TACACTTGAA ACACAGTGAG 480 AACCACCATC CGGCCAAATC CCCCAGCACT GGCGCATGGA CAACTCGAGA TTTCCCTCCT 540 CTTCTTTTTT TCTTTTTTTT AAATTAATTT GCAATGTCCC ACATGCTTAA CACTTGCCTT 600 CCTCCCTGGA TCTGGCACTA TTATCTTTAG TATTGTTTTT CTGGCAGTTT TTATGCTTGT 660 TTTTCCAACT ATGGCAATTT CTCAATCCAC TACATACCAT CCCTCTCAAT AAAACAGTTC 720 TCATGGAACG CAGCGGCCCA GAAGGACTTG GCCAAAGGCC TCTCCTGGGA CACAGCCCTG 780 TCTGTCTGCA CACTCCCTGC GCCACCTGGG TCATGGTCAC CCCAGATACA GAGGAGAGGC 840 TTCCATCCAC CACTCATTGA GCCCCCGACC CTCTGCTGAT CTTGAGCTTG TATTCCAGCC 900 TCGACGGGAG CTACTCTGGG AGGTGTTTCT AGTGTGATGA TCATTACATC CCAAATAGCC 960 CCCATTTCAC TTAAGAGGCT GAATGGACAA ATGGACAATG 1000
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