| Tag | Content |
|---|
EnhancerAtlas ID | HS062-01393 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr1:204131470-204132610 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:204131792-204131811 | AGGCCGCTAGGTGGCAGCA | + | 6.23 |
| | | 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 |
| GH01I204162 | chr1 | 204131621 | 204131870 |
| Enhancer Sequence | GAGTCAATTT AGAGGAGTCA GCTGCCCGGG GATTAAATAA CCCTGAAGTG ACTTCCTTCT 60
GTTGCCTAAT TTTGATTAGA CAAGGCTATT TGTTTATTGG TCCGTTCATT CATTTATTCC 120
GTAATCACCT GCTGAACAAC TACTTTGTGC CTCACTGTGC TGGACACTGG AGCTAGAAAG 180
ATAATGATCA TGACTGCCTT TAAGGAACTC CACCTGGCGG GAGGACAGAC AGGAAACAGG 240
CACAGACATT CCCTCTGAAG AGATTAATGC CAGGGAGTGC CCCTGTCAAA ACTAGGGGCT 300
GGCGGGGAGA CAGTGCCATG GGAGGCCGCT AGGTGGCAGC AGATGCCCAC AGCAGCTGCA 360
AGGTCTCCAG GATACCAGGG GACAGGCACC CAGCCAGGGC TGTGGTGGAG TGGACCCCCT 420
GAGCTGGGTT GGGCCTAGAG AGATGCCAGC ATCTTCAGAG CGCCATGCAC CTCGTCCTTG 480
GAGAGATGTG TCCCGGTCCC TTGGCTTCTT GTCTAGATGT TTTCCCATCA CCTTTGAGAG 540
GCAGAATTAA AGAGACCTAG GAAACTGACT CTACTGAGCC GCTACTGAAA TCACACCAAC 600
AAGCTAGCTG TCATCCATTT TATAGATGAG AAAAATGAAG GCTCACAGGG ACAAAGGTGA 660
CTCAGAAATG TTGAAGCAGG GATTCAGAGC ATGTGTCTGG CCCTATTTCC CATATAGGGT 720
CCCCTGGGTC CCGACATAAA GGCTGCCAAA GCCCAGAGGA AGATGTCTCT AGCTGTTCAC 780
GGGAAGGTCC CAGGATGGAA GCCCAAGTTG ACTCTGCAAT AGACTTTCCC ATACACACAA 840
AGATTCCCTC TTTCTTCTAC TTTCTTCTCA GTGGCTAGTC CTCCTATACT CACACTACCC 900
TTTCCTTCCT ACATCCTTCT TGCGTCCCAT GCATTCTACT TACCCCCATT TTGCCCATGA 960
ACATGAATGC AACTTTTATG CCTATCAGCA TGGTATTGTA ACAGAAATGA TTTGTTATCT 1020
TCCTATCACA GGTTACTGTT ACCAAAATAT TTTCACAATC ATTATTTTAT TTGCTCTCAT 1080
AAGGTGGATG ATTTTATTAC TCCCACTTCA CAGCTGGGAA CGTGGAGGGT CAGAGGTTTG 1140
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