| Tag | Content |
|---|
EnhancerAtlas ID | HS059-39935 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr6:35490180-35491350 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:35490767-35490786 | TTACCACCAGGTGGCGACA | + | 7.33 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 35490825 | 35491257 | | chr6 | 35490232 | 35491229 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH06I035522 | chr6 | 35490389 | 35491340 |
| Enhancer Sequence | CTGTCACTCT GGCTGCCCAT CAGGATCCCT CCTGAGCCTT ACAGCGCCCT AGACTGGTTC 60
ATCAGAACCC CTGGTGTAGG GCCCAGGCGT CAGCATTCGT CAAGGATCCC CAGGTGAATT 120
CAATGTCCAG CCAAAGCGGG GAACTACCAG GGTAGAGGCC TTGTGGCTTA TTGGAAATAG 180
TTGTGGGTTA AAACCCACCT GGGCTTGAGA CTTGGCTCCG TCATTTCAAG CTGTGTGACT 240
CTGCGCCAGT CACTTAATTT CACTGAGCCT CAATGTCCTC AGCTGTGAAA AAGGGGTAAG 300
TCCCTCTACC GTACAAAGGG GTTGTGAGGG TGGAATGAGA CAGTGTCTGC AAGGACTCTA 360
GCACGTAGGC TCCATCTTTA CTAGTAAGGA GGGGGCAGGA CAGACTAGGC TGGCAGAGCG 420
GAGGCAACGA CTCATCATCG CTGGAATGGG TCTGTGGAAT GTGTTGGGAC CCCCGAACCC 480
CAGGCCCTCC CACCGTGGGC TTTCAGCTCT TCCGGGAGCT TAAGGCTTCT GACGGGGGCC 540
AGCCCAGGCT TGGAGTGGGA GGGCGGGGAG GGTGCACTGA CTTAGCCTTA CCACCAGGTG 600
GCGACACGAA CACACCCACC GGGGAGGACA CCGGCCCCGC GGAAGGTGAG GATAACTGGG 660
AATACCAGGC ATGTTACAGG ACTTGGTTTT GGTTTGGTTT GGTTTTAGTA CTAGGTACAT 720
ATTTTCTTTC ATTTCCATTG ACTTCGTGCC ACAGTCCTGT GGTAGCGCCA CTGCCCTCCT 780
TTAGCGGGTG AAGAAACTGA GGTGGTGCTG GCAACTAGGA TGTGAACTCC ACATCCGCTT 840
CCTGACCACG GAGTCAACAG CAGTCAGAGC TGCAAGGGAA AGCGTCAAGT CCCGCGGTTC 900
CTAAACCTGT CTGATGATAA AAATCATCCA AGGCTCTTAA AAAAAAGAAG AAAAATATCC 960
TGGGCCACAG GCCAGATATT GAATTAGAAT CTCCTGGGAA AAGAGGCCTG AGAATGTGTG 1020
TGGTTAAGAG CACCTGGCCG GGCGCGGTGG CTCACGCCTG TGATCCCAGC ACTTTGGGAG 1080
GCCAAGGAGG GAGGATCACT TGAGGCCAGG AGTTCAAGAT TAGCCTGAGC ACATAGTGAG 1140
AGCCTGTCTC AATTTAAAGA AAAAGTTAAA 1170
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