| Tag | Content |
|---|
EnhancerAtlas ID | HS175-02849 | Organism | Homo sapiens | Tissue/cell | SK-N-MC | Coordinate | chr1:222945620-222946770 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat4 | MA0518.1 | chr1:222946297-222946311 | CTTCTAGGAAATAG | + | 6.36 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 222945905 | 222946742 | | chr1 | 222946400 | 222946600 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I222771 | chr1 | 222945143 | 222947142 |
| Enhancer Sequence | GATCATCTGG TTTCCCTGGC CCCTAGGTGG GGACCATGGA GCGAACTGGA GAAGCAGGCT 60
GGGTCCTTCC TACTCCTGAG GCTGGCAGAG CACACTCTAT AGCTGAGGAG ACTGGAAGTT 120
AAAGGGTTTC TTCACAAGCA ACTGACAACT TGCCAGCTGT ATGTGTCTTC TTCTCTCTCT 180
CTCTCTTTTC TTTCTTTCCT TCTTTTTTTT TTTCTTTTTT TAAATTAATT CAGAGTCTCG 240
TTCTGTTGCC CAGGCTGGAG TGCAGTGGTG CAATCTCGGC TCACTGCAGT CTCCGCCTCC 300
TGGGCTGAAG AGATTCTCCT GCCTCAGCCT TCTGAGTAGC TGGGATTACA GGCACACATC 360
ACCACACCTG GCTAATTTTT CTATATTAAG ACGGGGGTTT CACCATGTTG GCCAGGCTGG 420
TCTCGAACTC CTGACCTCAA GTGATCCACC TGCCTTGGCC TCTTAAAGCG CTGCGATTGC 480
AGGCATGAGC CAGCGCACCC AGCCGTGTAT GTGTCTTCTT ATTGCTCACT GAATGGCTGC 540
TGCTGAAAGC ACACTAAGGA AGTAGATCTG AGTCCCAAGG GTGCATAAAG CCATGTGAAG 600
GCAAAATTAT ATAACGCTGC ACTCAGGAAG ACTAACAGCC AGATAGAAAC AACAAGCAGA 660
ATACACAGAA CAGGCAACTT CTAGGAAATA GAACTTGAAC AAAAAATTAC AGCAAAGGAC 720
TTTCTAGAAC TAAAAAGAAG AACTCTTATA TTCAAAATTT AGTAGATAAA TTGAAGGGAA 780
AAGATACTCA CTGTTGAAAC ACTAATTAGT TCCCCAAAAG CTCAAGTTGA AGCAGTATCT 840
CAAAGCCCAG GGCAAAAAAT ATAGAGAAGG AAATGTGGTA CAGAAAACAA AAACAGATGG 900
ATTGCCTGAG GCCGGAAGTT TGAGACCAGC CTGGCCACAT GGCAAAACCC CGTCTCTACT 960
AAAAATACAC AAATTAGTTG AGCGTGGTGG CTCACAGCTG TCATCCCAGC TTCTTGGAAG 1020
GCTGTTATGA GAATTGCTTG AACCCAGGAG GCGGAGGTTG CAGTGAGCTG AGATTGTACC 1080
ACTACACTCC AGCCTGTGCA ACAGAACAAG ACTCTGTCTC AAAAAAGTAG AAGAAAATAA 1140
AATAATAAAA 1150
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