| Tag | Content |
|---|
EnhancerAtlas ID | HS062-09022 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr2:62019900-62021360 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:62020602-62020621 | CATTGCCACCTGCTGGAGA | - | 6.29 |
| | | 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 |
| GH02I061793 | chr2 | 62020434 | 62020954 |
| Enhancer Sequence | GTCAGTGGCA TCATCTTTAA TATAAAAAGC CATAAAGGGT CCCAGTGTGA TGGCTGATGC 60
CTGTAATCCC AGCACTTTGG GAGAGCGAAG CAGGAGAGAA TCACTGGAGC TCAGGAGCCG 120
GAGACCAGCC TGGGCACCAT GGCGAGACCT CCATCTCTAT AAAAAAAAAA TAAATAAAAA 180
GTTAGCTGGG GTGCTGGAGG GCGCCTGTAA TCCCAGCTAC TCGGAGATTA TCTTACCACT 240
GCACCCCAGC CTAGGCAACA GAGTGAGACC CTATCTCAAA AAAAAAAAAA AGTCATAAAA 300
TTTAGGATTC TATTTCTATG AGCATTTTAA GATGCCTTCT TCTTGTTCGC AGCTCCTAGC 360
ACCTTTTATT TTATTCTAGT TTAAGCAAAA TTTAAATATT TTTAAGGTTG GCGGTTAAAA 420
TAACGAGGTC AGGAGTTCCA GACCAGCCTG GCCAATATGG TGAAACCCCG TCTCTACTAA 480
AAATACAAAA ATTAGCTGGG AGTGGTGGCG GGTGCCTGTA ATCCCAGCTA CTCGGGAGGC 540
TGAGGCAGAA GAATCGCTTG AACCCGGGAG GCAGAGGTTG CAGTGAGCCG AGATCATGCC 600
ACTGCACTCC AGCCTGGGCG ACAGAGAGAG ACTTCGTCTA AGGAAAAAAA AAAAAATGTA 660
AATATTTGTG CCTTCTGTCC TCTTTGGAGG CTGACACTAA CTCATTGCCA CCTGCTGGAG 720
AAGAGAAGAC GTGCAGCCAG ACACCTGCCG CCTTGTCAGG CCTGTGTCGC CGCCTCCGCA 780
GCCCGAAATC ATCCTGCCCT CCAAGGCACC GCCCTGATGC TCCAGGTGAA GGCTGAAGAA 840
TGGTATGTGC GGTGGGCTCG GGCAGAGGCG GGTCCTCGCC CTTTCCATTC GTGTGAAGTG 900
TGGTGTGTGT GACCTGCACC CATCCCTTTA CTGTTGGGGG TGGGCACCCC GGCGAGCCGC 960
AAAACAGCAG GCGGACTCCC CTACTGGAGA GAAGCCGGGG AAGTGCAATG GTAAGAGAAG 1020
CGGCGGCCAC ACCTGCTGCT GTGAGGATCT GAGCAGGGTT GGTTTTCTGT TTGTGCGCGC 1080
GCGCGCGCGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT TTTAATTATA CTTTAAGTTC 1140
TGGGATACAT GTGCGGAACC TGCAGGTTTG TTACATAGGT ATACATGTCC CATGGTGGTT 1200
TGCTGCACCC ATCAACCAGT CATCTACATT AGGTATTTGT CCTGATGCTA TCCCTCCCCT 1260
AGACCCCACC CCCGGACAGG CCCCGGTGTG TGATGTTCCC CTCCCTGTGT CCATGTGTTC 1320
TTATTGTTCA ACTCCTGCAT ATGAGTGAGA ACCTGTGGTG TTTGGTTTTC TGTTCTTGTG 1380
TTAGTTTGCT GAGAATGATT GTTTCCAGCT TCATCCATGT CCCTGCAAAG GACATGAATT 1440
CATCCTTTTT TACAGCTGCT 1460
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