| Tag | Content |
|---|
EnhancerAtlas ID | HS069-07696 | Organism | Homo sapiens | Tissue/cell | GM18951 | Coordinate | chr7:42980400-42981630 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr7:42981031-42981050 | GCTCCACTAGGGGGCAGCA | + | 6.44 |
| | | 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 |
| GH07I042940 | chr7 | 42980550 | 42981412 |
| Enhancer Sequence | CTCCCACTCT CCTCAGATAA CTGTTTTCTA CACCTGCCTC CACCCTCCCA TATGCAATTA 60
TGTTTCAGGG GCAGGATTTG CCCCTCAATA TTTCTAAATC TGTGCTAAGG AATTCTGCTA 120
CGATTAGTGT TTTTCTGGCA AATACACAAA CATAGATGCT CTGTCTTCAA CTGCAATTTT 180
TAGGGAGCAG TGTCATTCCA TGGTCTAGAT TAGTGAATAA CATTTCCATC TTGCCTTTGA 240
AACAGGATGG TGTCGCTTCC AGCTGCTGTC CTCTCGTTTT TTCCACAAAG GGCATCCAGA 300
ACAGCAACAG CTAAGGCAAA TAGAGAGATA TTCCCTGGTG CTCAGTGGAA TGTCCCTGGG 360
CTACTCTTTA CCTTACTTCC AACCTTCGTG TTACCCTGCC CCTGTGTTCC TCTGCTGGCC 420
CCGGTGACGG TCTGTGCACT CACCTCCTCC ACGTTTGTGG AGTCGCTAGT AAGCATTAGG 480
CATGCAATTT GGAGGTAGGA CAGGAAGAAA GCTAGAGGGT TAACGAGTTC CAGTCTCTGG 540
ACCCTGGTGT TCAAGCTCAG AGCCAGCTTT ACAGTTTCAG CCTTTAAACT CACATGAGGA 600
ACTGCTACAG TTTACTAGGC ATCAGCAAGC CGCTCCACTA GGGGGCAGCA GGTGAATTGC 660
ACTGAAATTC TCAAATGAAA TAATAAACCA TCAGGTACAG CAATGCTGGG GACATTGTCT 720
GTTTCTGCCA AAGCCATCAG CCTGTGGCTA GCAGACAGGA TTACTGCAGG GGGAGAAAAG 780
GCTGTCTGCA ACGCTGAGTG AAAGCTAGAG GCTGCCAACA AAACTGAGCC TCCCTATCAC 840
TGTGTCCAGG GCTTCTCTCC CTCCGCCCTG GGTCAGTTTG CTCTCGCCAG TGTTCCCTCC 900
TTGATCCTCT TCTTTTCCAA CCCTACATCC TTGGGTACAT GCAGCCAGCT TAATTCTAAA 960
ATCCTTTCCA AGAGCATCTT TCAGGATAAA AACTCTTTTC CAATATTCCC CAATATTACA 1020
TTTCGGTAAC TAAAAAGAAC TACTGATTTT CTCATTGACA TTCTTCTAAT CAGTAGTTCT 1080
CAACCAGGGA TGATCCCCTT CCCACCCCAG AGGACATTTG GCAATGCCTA CAGACATTTT 1140
TGGTTGTCAC GCTGGGGTAG GGGGGTGAGG GATGATGAGA GCTACTGCCT TCCAGTGGGT 1200
AGAAGCCAGG GACGATGCTC AATATTTTCC 1230
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