| Tag | Content |
|---|
EnhancerAtlas ID | HS184-30293 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr8:125437490-125439000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr8:125438416-125438435 | TGGCGCCCCCTCGAGGCCA | - | 6.87 |
| | | 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 |
| GH08I124425 | chr8 | 125437443 | 125438990 |
| Enhancer Sequence | TACAAGTCTG TGGCCTGCGT CTCTGAGCAC AGGGTGGCTT TCCTGGAATC CTGGAGGAAT 60
GGAATTGGGG GATCCAGTCT TGTCCTCTGT TGATCAATAT CTTCTATGGT TCCCTATCAC 120
CTTCTGGACT AAGCCCAAGG CCTGCATTGT CCTTCCAAAG CCTTTTGAGA TCTGACCCCT 180
ATCTATCATC AATTCTCCCT GAGCACCCCC TAGTGGTACT TTAGGCACTA GCACTGTCAA 240
AGTCCTGTTG ATGTCCAATC ACCCATATTC TCTCGCGCCC CCACTCCCCC ACCCACCATG 300
CTTATGGACA CATTGTTCCC GCTGCCTAAA TGACCATCTG GCAAATGAAC CTTGTCTGTG 360
AGCAAACGTT TCCTTTCATT TATCCTACCT CACTGCCTTA GTAAAACATG CCCTCAGATT 420
ATAGGTTCTC CTCTCTATCT GCTCTACAGC ACTGGTGATT CTGTAATTAT TCTAGTGAGG 480
ACCAGCTACA TAATTCGTGG GGTCCAGTGC AAAATGAAAA TGAGGGGTCC CCTTGCTCCA 540
GAATGACGGC ATCTGTTTGC CATGTACCTG GATGCAACCT GCCCCTGGGG AGCTGCCCTT 600
GCCCCATCCT TTTGAGCCAT GGCACGGTCC TGCATCTCCA ATACCAAATC TGACTCCAAA 660
ACTGTGTGGT GTGACATACA AGTGACTGAA CGCTTCCTGG GGAGCTGGGG TTGGGGGCAC 720
TTCAACCACC ACACAGCACA GCTTCATCAA AATGCAGCTT GCGACTTCTC CCCCAGGTGC 780
CTTCCCGCTG CTGCGGGCCT CTGCTCCTTC ACTTCCAACA TCTCTCAAAA TAAAAATCCC 840
TCCTCCCGCT CTGAGCGATT CAGCTCTGCC TGCAGCTTGT ACATGTCTCT CCCCTGGCAA 900
AACAAGAGCT GGGTAGTTTA GCCAAATGGC GCCCCCTCGA GGCCACTGCA GGTCCTTCAT 960
TCACCCCGTC ACATACAGAG GGGTTCTGAG TAAAAACAAA ACGTTCTGCC GCTCAGGCCA 1020
GTGTGGCAAA CACTCAGCCA AGCCTCAGGA TCCTTCCGGG GAGAGTGTAG GTAGACAGTG 1080
TCCTGCTCGG GGGGCAGGGG TGTCCCAAGG GCTGGCCCGC CTGCTGTCTG CTCCTCCTGG 1140
CCCCTGGTCA GGCGGCAGCC AGAGTCCCTC TGGACCTGCA TCCTCGCCCC AGCAGAAGTC 1200
TTTTGTCCAG GGGCCAAAAA GCCAGAGATT CCGCAACAAG AATTCAAAGC AAACACAACA 1260
AAACAAAATT CATGGAAAGT AGATGACTGC TAAGATATGG CAGGGGGGCC TGGAGGGAGC 1320
CTCCGGCTCT GACCTGCTCT GGGACGGGCC GCCTTCTCCT CCGCATGTTG CTCAGTTTCT 1380
GCCCCTGACG CTGGAGCTCA CAGAGACGAC TTCCTTGTCC TGGTTCTCAA CAGAGCTGTA 1440
GCTGACTCTG GCATTACCAA GCCTCCCCAC ATGCCCAGCC CCCTCACTCC AAAATCCTAC 1500
TGGCTGTAAC 1510
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