| Tag | Content |
|---|
EnhancerAtlas ID | HS098-10001 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr11:56991090-56992760 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Pou2f3 | MA0627.1 | chr11:56991639-56991655 | TTAAATGCAAATTAGA | + | 6.19 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH11I057224 | chr11 | 56991738 | 56991923 | | GH11I057225 | chr11 | 56992141 | 56992290 |
| Enhancer Sequence | GTCACCAAAG ACCTCTGTGT CACCAAATCC AGTGGATCGT TTTCTGGTTT CCTCTTATCT 60
GACCTCTCTG TAGGATTCTT CACAGTTCCA TCTCTATGAT GTTCAGATTT TTATCATCAG 120
TCCAGACCTC TCTTCCATTA CATATCAAAC TGCCTTCTCA ACATCCGCAC TTGAATGTCT 180
TATTAACATC TCAGGAATGA TATGGTGATG TAGCCAAAAC CTAAGCTATT CTTTCTCCAG 240
CCTTCCCTAT CTCACTAATT GGTATCACCC TCTTCCCAGT TGCTCAAGTC AGAAAGTTTG 300
GATAATTCCT TCTTTCTCAC CCCCTCATCC ACCCACTCAC TCAAACCCAG GCGATCAGAA 360
GTCCTATTCA TTCTGCATCA AAAATATAGC TCAAACCTGC CTCTCTTCTC AGTTGCTGTG 420
GATACCACCC TAATGTGACC CACCAACATC CCTCATCTTG GCCTCTGAAG TAGCTTCCTA 480
ACCGGTCTCT CTGCTTTCCC TCCTACTCCC CTTCAACTCA TTCCCTATGC AACAGCTTGA 540
GGAACAATTT TAAATGCAAA TTAGATTGTA TCATTTTTCT GATGATTTCT CATTGCATTT 600
AATAAAGTCA CACTTCTTAC CACAGCCTTC AAGGTCCTAC ATGACCTGGC CCCTTTTTGG 660
CTCTCTTTGT CTCAGGCCAC CCCCTGCCTG GCTTCCTGGG ACTAGCCTTC CAGTTGCCCT 720
GACAACCTTC CCAGAACCTA CTGTGATCTT TCTTGCTTCA CAGTCTCTGC ATTTGCTGTT 780
TTCTGCATCT GGGACTCTCT GAGCCTCCGT TGCACAGGGC AGGCTCATTC TTATTCTTCA 840
GATGTCAACG GAAAGGTCAG CTTCCAAGAT GGCCTTCCCC AAGCACCTTT TCTGAAGTTG 900
TACTTAATAT TATTTTCCAC TTCAGATGTT ATTTCCTTCA TAGTATGTTC CATAACTGGC 960
CATTTCATAA AATGGCCAGT TTATGTATCT GTGTATTTTC TATCTTTCCC TACAAAAATG 1020
CTAAGCTAGA CAAGGTCTAT CTCATCACTA TAATCCTAGT GGCTAGCTGA GTGAGTGGCA 1080
CACAGTAAAT GTTCAACAAG TATTTGATGA ATGAATGAGT CATCATGATT TGTCCCCAGT 1140
CTAATCCTTC CTCCTTTATT CCACATTCCT TTGTATGTAT ACCCAACACA CAAGCTAGTC 1200
AACTTGCTCC TCAGACCTCC TATGCTCTTC CTTACCCTCT TTCACACTGT CTCCTCAGGC 1260
TGGATGCCTC CTACCACCCC CATTCCACAT TCAAGTCACC AAAATCCTAG TTATCCTTTC 1320
AGGCCCATCT TCAACTCTAA TGCCTGAGAT TCCACCATTA GCCATTCTTA GAATTATAGA 1380
ATGTCAGCCC TTATAGATGG TGGATCAAAA TTACATTTAT CATTTCAATT GCCCAGAGTG 1440
CTGCATGGAG AGGGATTATG AGTTTTGGCA CCACAATCAT ACCAGAAAGG CCATCCATAA 1500
CAATAGGAAG GTTATGACTG TCCCAATCTT TTTCAAGCTC CTCATGATAC AGATGGGAAA 1560
ACTGAGGTTG AGGCAGGTGG CATGACTTCC CAGGGAACAC ACTAAGTAGG AGACGGTGAT 1620
GGGAACAGAG TTTCCATCTC TACATCACCA GTGTGGAATT ATATCAGGCT 1670
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