| Tag | Content |
|---|
EnhancerAtlas ID | HS052-19906 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr2:27407820-27409230 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr2:27408145-27408156 | CTTCTGGGAAA | + | 6.62 |
| | | 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 |
| GH02I027183 | chr2 | 27406528 | 27409317 |
| Enhancer Sequence | CACTGCCTCC GAAACACACA CACACACACA CACGACACTA GCCACCCTTA GGCTCATGTG 60
AAAATGCTGG GCTGTGTAAA CTGGAACTGC CTTGAAAAGA TGGAGGTGCA TCCCCCAATA 120
GGGTTGGCCA GATTTAGCAA TAAAAATACA GGATGCCCAA TTAAAACTGA ATTTCAGATA 180
AACAATGAAT AGGCAACCCC AGGCACTGAG GATGAGCTTC GATTAAGCCA AGTGGTAATC 240
CTCTCCTCCT TGCTAGTGAT TAGTTTGGGA GTGGGCTTAT AACACAGTTC TGACCAATTG 300
GAGCAGAGGA GAAATCTTCC AGGGGCTTCT GGGAAAGATT TTCTTCCCTG ATTAAAAACA 360
GAGAGAGTGT GTGGAAAGTT CCTTATGCTT CCTGCCTTCA ATGATCATCA TGTGAAGATA 420
TGGTGCTGGG AACAGCAGAG ATCATCTTAT CACCGGGAAG GGAAAGTCAC GAGAAAGTCA 480
GAGAGACTGA GCCAGAACTC TGACATTGTG GAACTTCTGA ATTAGGCAGC TCTGGAATTC 540
TCTTTTCCAG GACTTTTATG GGAAATAATG AATGTCCTCA CTGTTTGAGT CACTTTTACT 600
TGGGTGTTCT GTTTGTGCTG CTGAAAGCAC CCTCAATGAT TTAGCTGAAA GTTTTTGAAG 660
CTCACTCAAC AAGTATTAAA TTGCTGTGGT TAGTAGATCC AGAACTCGGC TAAAGAAACT 720
TATCTCACTC AAATAAACAA AATTATTTTA TTATGAGATC CACTGGCCCA AAAGTGTTGC 780
ACGAGTCTTT CTCAACTTCT CACGGTTTAG GAATCACAGA AACCCTCCCA CAGACTTTGA 840
GAAGTGGGCA GGAGACAGGA TGGATTGGCT GTTCTTGTTA ACAGTTCTCA GTGTCCTTGC 900
TGTCATTGAC AGCTTCAGAG ATCTGAACTG GCTTCATGAG GAAGTGCTAG CCAGGCAGGC 960
CGATTCTGTG GGACAGATGG CTGCTGTTTC ACAATTGTAG ACATGAGAAG GGCAACCTTT 1020
AGCCCAGAAG CTGGGGTTGG TGATCCTGAG ATATCATTAG CATCTATGGC ATCTGTGCTG 1080
TCACTTTTGA TCACAGTGTG GATAGTACTC ACTGTTCATT TGTTTTATTT CTAAACATTC 1140
TAAAATGAAT GCGATTTATC AAATGTTTAA CAGCACAATT CTGACATATG GCAAACTTTT 1200
TTTTTTTTTT TTTTTGAGAA GGAGTTTTTG CTTTGTTGCT CAGGCTGAAG TGGAATGGTG 1260
CCATCTTGGC TCCCTGCAAT CTCTGCCTAC TGGGTTCAAG CGATTCTCCT GCCTCAGCCT 1320
CCCAAGTAGC TGGGATTACA GGCGCCCATC ACCATGCCCA GCTAATTTTT GTATTTTTAG 1380
TAGAGATGAG GTTTCACCAT ATTGGACAGG 1410
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