| Tag | Content |
|---|
EnhancerAtlas ID | HS176-02695 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:169714000-169715260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr1:169714629-169714643 | ATTCCCTGGGGAGT | - | 6.82 | | EWSR1-FLI1 | MA0149.1 | chr1:169714708-169714726 | GGAAGAAAGGAAGAGAGG | + | 6.7 | | STAT1 | MA0137.3 | chr1:169715074-169715085 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr1:169715074-169715085 | TTTCTGGGAAA | + | 6.32 | | Stat4 | MA0518.1 | chr1:169715074-169715088 | TTTCTGGGAAACAG | + | 6.14 | | TCF7L2 | MA0523.1 | chr1:169714543-169714557 | GGCCTTTGATGTTC | - | 6.3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 169714454 | 169714700 | | chr1 | 169714203 | 169715000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I169744 | chr1 | 169714009 | 169715527 |
|
Enhancer Sequence | CTCCCAATGT GCTGGGATTA CAGGCATGAG CCACTGCACT CACCAAGCAC TTCTACTGAT 60
AGCATTTACA AACCCTTCTT AGAATATTTA AAAATTCTAA GAGAAGAGTA AATTGAGCCT 120
TCCCAACTAA TACTAGGAGG TTATAACCTT CATACCAAAA CTGGACAATG CTTGCACAAA 180
AGAAGGAAGC CAATGAGGCC ACCTAGAAGG AAGACTGGGC ATTGGGCCCA GTGAGTCCTG 240
GAAACCTCAT CTGTGCCAGC CACCCCGGCA TGGCCTGTAT GAGTGGATGA GGGTGACTTG 300
TCCACAGACA ATAGCCATCT AGCTGTGATA AAGGAGTCAA GGTAGTCAGC TGCATCTCTT 360
TCACCTGTTT GCCAATGTTA CACAGGTTGA AAAGCTAAGG TTTATGTAAA GCAAGCATCA 420
AAGATGATGA AATGATCAAC CTGACAATGA GTACTATGCT GCATTGTCCA GAAAGGAACT 480
GTGGAAGATT TTGGGCTGAA TTTCAAAACA GAATTTCCTC ACTCTCTGGA TGTTGGCTTA 540
CTTGGCCTTT GATGTTCAGA GGTGGTGCCT TTGTGTTGTT GAACAATGTT GATTTTGGAG 600
AGAAAACAGA GTTGAAAAAC CCACAAGTCA TTCCCTGGGG AGTATTACCG GAATACAGAG 660
GATAATTTCA GCAAGCCAGC AAGGCCTCAT CTCTGCTTCT AATAGATAGG AAGAAAGGAA 720
GAGAGGAACA ATACTTTTTT AAGAAGCTCA GCTTTATCGC CTTATCTCAT AGAAAGATGC 780
CTCCAGTCTG TCTGGCTAAA GGTAATTGGC ATGGGAAAGT CTTTATCTGT GATTCTAACA 840
AGTGGAATGT TTCCCTTCAT TAAGAGAGCC TTGTCTGGCT TGGGGAAATG AAACACTTTC 900
TCCGATATGA GTGGGCTGTA ACCCCTGCTA CTAAATACTC AGAAGAAATA AGGCGGTTGT 960
GGAGCAGTCA GGAATGAGTC ACTTGCCTCC CTGGAATATT CAGAAAACTG AATCAAAAGT 1020
ACATTCTTCT GGGTTTTCTT AGTCTAATAG ACTAAGGGTC TCTACTTTGT TAAATTTCTG 1080
GGAAACAGCA TAGAATGGGA GAAAAAACTG GTCACTGTAG TCATGCAAAT CTGCAAAACA 1140
AACAAAAAAG TCTGGGTATT GCTGCTAACT AGCTATGTGA CCTTAAGCAA GGTATTAACT 1200
CTCTCTGAAT TTCAGGTTCT TCATCTGTTA AATAGCATAT CTGTAAAATG GGAATTATTT 1260
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