| Tag | Content |
|---|
EnhancerAtlas ID | HS034-29581 | Organism | Homo sapiens | Tissue/cell | ECC-1 | Coordinate | chr8:103917940-103919360 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr8:103918730-103918744 | GGAAGGTGACTCAT | + | 6.27 |
| | | 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 |
| GH08I102905 | chr8 | 103917800 | 103920335 |
| Enhancer Sequence | AGGAGACTGA GGCAGGAGGA TCACCTGGAC CTGGGAGGTC CAGGTTGCAG TGAGTAAAAG 60
AAAAGAAAAC TGAGACCCAT GGAGGTTAAG TAACTTACTT TTAATCACTG TTACTTATTT 120
TTTTCTCTTT TTTTGAGATG GAGTCTCACT CTGTCGCCAG GCTGGAATGC AGTGGCGCGA 180
TCTCTGCTCA CTGCAACCTC AGCCTCCTGG GTTCCAGCGA TTCTCCTGCC TTAGCTTCCC 240
AAGTAGCTGG GACTACAGGC GTGCACCACC AAACCCAGCT ATTTTTTGTA TTCTTAGTAG 300
AGACGGGGTT TCACCATGTT GGCCAGCATG GTCTCAATCT CTTGACCTCG TGATCTGCCC 360
GCCTTGGCCT CCCAAAGTGC TGGGATTACA GGCATGAGCC ACTGTGCCCA GCCCAATCAC 420
TGTTACTTTT AAGGAAATCC ATTTGACTAC TAAGGCATAA TGTCACAGTG GCTTAGACAA 480
AATAGGAGTT TCTCTCTCAT GTTAGTCTCA TCATGAGCAG TCCAGGGCTG ATAAGACAGC 540
TGAGTCTTGT TGGGGACCCA GGTTTCTTCT TTCTTGTTGC TCTGCCTTCT CTAGGGAATA 600
CCCTATTCCA CCTTGTCAAA GATGGAGCAA TGCCACCTCT GCATTCCAAT GGAAGAAATG 660
GGAGGAAGTG GAAGACACAA CCTTCCCTTT TAAGGGCATA ACCTGGAAGT TGGGCTCATA 720
TTTCAATGGC CAGAATGTGG TCCAATGGCC ATACCCAGTT GCAAAAGAAT CTGGGAAATG 780
TAGTCTGACT GGAAGGTGAC TCATACAGCT AAAATTCAGG GAAGAAGGCG AGAATGGATA 840
ATGGAAAACA AATAGGAATC TCTGTCACAG TCAGAAGTCG AACTGGGATT CAAACCCAAC 900
AGTTTGACTT CAAAGCCAGA ACTCTTAACC ATAATCTTCA TTATGCTGTT GTTTTAGAAG 960
AATTAAATGA GGTCCACAGT TGGTAAGGTC TTTCTCTACA GTTTGAGACT TCATTAACAC 1020
ATGTATGCAC ATACATTTTT GCTAAATGGA TAGATTATAG CTGCTCTTGC CATAATATTA 1080
TAACGCTTAC TGTGAAAGTT GTTCAACATT GATGGGGAAT CAAGTAATGT TTCCTTTTTT 1140
TTTCTTTTTT TGTTTTTTTG CCTTGAGACA GGTTTTTACT CTATCACCTA GGCTGGAGTG 1200
CAGTGGTGCA ATCTTGGCTC ATTGCAGCCT TGACCTGCTG GGCTCAAGGG ATCCTCCCAC 1260
CCCAGCCTCC CAAGTAGTTG GGACTACAGG TGTACGCCAC TTGTAGTCAA AAAATAAAAA 1320
TCAATTTTTA AAAACTGATT TGTAGAGGCA GGGTCTCTCA CTATGTTGCC CAGGCTGGTC 1380
TCAAACTCCT GGGCTCAGGT GATCCTCCTG CTTCCCTTCC 1420
|
| |
|
|
|
