| Tag | Content |
|---|
EnhancerAtlas ID | HS052-19144 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr19:46133810-46135190 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr19:46134019-46134032 | CTCATTTGCATTT | + | 6.28 |
| | | 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 |
| GH19I045629 | chr19 | 46132886 | 46136602 |
| Enhancer Sequence | AAAAAAAAAA AAAAAAGACC TTCAAAGGCC CTGGCCATTT TGCAGGAAAC ACATTAAAAT 60
ACACCCTCCA TTAGAAGCTG TGAAGACATC TGAAATGGTT TCATACTATG CCTTGAAATG 120
ACTCATCCCT AATAAACTCA TTTCATTTGC CCTCAGCTAT TGTTTCTCTG CAGCCAGCAC 180
CCCTAGCCAG GAATTCTTGC TGACATCATC TCATTTGCAT TTACATATAT AGAGAATGAC 240
TGATGTAGGT GAAATTCAGC AGTTAACAAA GTTGGTATTA TGTTGGGTTT TTGTTTGTTT 300
TTTATTTTAT TTTATTTTTT GAGACTGAGT CTCATTCTAT TGCCCAAGCT GGAATGCAGT 360
TGCATGATCT TGGCTCACTG CAACCTCCAC CTCCCAGGTT CAAGCGATTC TCCTGTCTCT 420
GCCTCTCAAG TAGCTGGCAC ATGCCACCAC TGCCCTCCTA ATTTTTGTAT TTTTAGTAGA 480
GACAGGGTTT CACTATGTTG GCCAAGCTGG TCTTGAACTC CTAACCTCTG GTGATACACC 540
AGCTTCCACC TTCCAAAGTG CTGGGATTAC AGTCATGAGC CACCTCGCCT GGCCAATGTT 600
GGGCTTTTAT ACCTTTCATT AAATACAGGT TAATTTTGAT TTGGCAAGGT TTTATTTTCT 660
TCTCCACACC TTTGGTAACA ATATGGCTTA CCCCTACCCC AAGCTCTTAA ATGTTTCTTT 720
AGGCCTCAGA AAACCGGTGA GGGTCCAATC CAGTGCCTCT TAAGCTATCT GTGCAGGAGA 780
CTGGCTGTTT TTTACTCCCT AATCCATTGA AGACTAATAT TTTAATCAAA TATGATAAAA 840
ATGTAAAATA TGATTTTTAT CTATCTATCT ATCTATATAT TTTTGAGACA GAGTCTCACT 900
CGGTCCCCTA GTGTGGAGTG CAGTGGTGGG ATCTGAGCTC ACTGCTACCT CCGCCTCCCA 960
GGTTCAAGTG ACTCTCCTGC CTCTGCTTCC TGAGTAGCTG GGATTACCAC ACCCAGCTAA 1020
TTTTTGTATA TTTTTAGTAG AGATGGGGTT TCACCATGTT GGCCAGGCTG GTCTCGAACT 1080
CCTGACCTCA AATGATCCAC CCATCTTGGC CTCCCAAAGT GCTGGGATTA CAGGCATGAA 1140
CCGCATCTGA CCAATTTTTA TTTATTTTTT AAAGTCAGCG TCCTGCCATA TCGCCCAAGT 1200
TGGAGTGTAG TGGCATGATC ACAGTTCACT GCAGCCTCGA TCTCCTAGGC TCATTCAATC 1260
CTCCCACCTC AACCTCCCAA GTATCTGGGA GTACAGGCCC AGGCCCACAC TAGTACACCC 1320
AGCTAATTAG AATTTTTTTT TTTTTTTTTT TTTTTTTTAG TTGGAGTCTC GCCCTGTCGC 1380
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