| Tag | Content |
|---|
EnhancerAtlas ID | HS083-01822 |
Organism | Homo sapiens |
Tissue/cell | HCC1954 |
Coordinate | chr3:127993170-127994440 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr3:127994241-127994256 | AGGGCTGTGTGACCT | - | 6.51 | | FOXF2 | MA0030.1 | chr3:127993748-127993762 | CTTGTTTACCTTCA | - | 6.27 | | KLF13 | MA0657.1 | chr3:127993649-127993667 | AAGACACGCCCCTCTGTA | + | 6.84 |
|
| | 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 |
| GH03I128273 | chr3 | 127992831 | 127995113 |
|
Enhancer Sequence | GAGGAAAGGG GCAAGCTGCT CTAGAGCACG CACGCATGTG GGCGCAGTCA CCACAGGAAG 60
CCTCAGCCCC TGCACCCTCT ACATGGAGCC CTGGCAGTCA GGCAGCACTC AGTGGTTGCT 120
GGGGGAGCAG ATGTGGAGGT GCCAAATGTG GCGCGGGTAG GGAGTGTGGC TGGCCTCTGG 180
ACATCCCCTG TAGAAGCCAC ATGTTGAGGG AGCCTAGGTC GGTGTGGGCC CTGGCCCAGG 240
GTGGCCTTGG GACACTCCCA GGGCAGCTGT AGCACCCTAC AAGTTGTCGT ATGAAAACCA 300
CTCTAACTTA TACGTGCTTT TGGGTGGAAT TAAATGAGTT TTATTGTTTC TAGGACAAGA 360
TAGGGATTTG ATTAGAAACA ACATTTATGG AATGCCAGGG CTGGTTCCCA TCCACTGTGC 420
CCTGCAGGAA CACAGAGTCT TGGGTCCCAG GCATAAACGG CCAGCTGTGT GACTGGGGCA 480
AGACACGCCC CTCTGTATGG CCAGGCCACC TTCTTAAATA AGTAAGAACA GCCTTCAGGT 540
GGGAATGGTT CTTCCCAAGG GCCATTTGCT TTCACAATCT TGTTTACCTT CAGTGGTCAG 600
TTAAGTTTCA AGGGGAAACT GTGACTCAGG CCAGTGGAAT TGTCAGATGC AGAAGCAAGG 660
GGTGAGATGG ATGCGGGCTT GCTGGGCTTA CCGAAACTTG TATGCCTGTA GGCCTCTGGG 720
GGTGCAGTCA TTTCCTCCCT CTAGCTGTGG GCTGCGGTGC CTTTGGAATA GGATGCGCAT 780
GTCATCGAGG GGTCTAGCAG TGACCTGAGG ACTGGCAGGA CCTCGATACT GGGGCCCAAA 840
GCGGTTTCCT CTCCTGGGAA ATGGGTGCCC AGCCAGTGTC AGAGCCCCAG CTGGGAGTGG 900
CCTTGGTGCA GAAAATGCTG TGTAAATGGC AATTGACAGT GCCAGGTTGT GCCCAATGCA 960
AGCATGGGTG CTGCCTGGTC CACAAAGGAG TATCTGATCT TTGACTGTCT GAAGACCACT 1020
GCCTTTCTAG GTTGGAAGCA AGCTCTGATT CAGATGAAAG TGTGGCCATG CAGGGCTGTG 1080
TGACCTCAGC TTGCACACCC ATGAAGCCAG CCCTGCCCAC AACCTTTCCA GATACTGTTG 1140
ATGCGTGTCA TGTCGGGGAC TGGAGTCCCT GACAGGTATC AGAGCCCAAG CTGGCCCTGG 1200
GGGAGCCCTC AGTGGGGCTG GGGTGGTCAG GCAGGCAGCT GTTTCTTCAT ATGGGGAAGG 1260
CACTGAGTGA 1270
|
