| Tag | Content |
|---|
EnhancerAtlas ID | HS034-11226 | Organism | Homo sapiens | Tissue/cell | ECC-1 | Coordinate | chr16:31093020-31094290 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr16:31093243-31093257 | GTGGGGGCGTGGTC | - | 6.01 | | KLF16 | MA0741.1 | chr16:31093245-31093256 | GGGGGCGTGGT | - | 6.14 | | SP1 | MA0079.4 | chr16:31093244-31093259 | TGGGGGCGTGGTCAG | - | 6.52 | | SP3 | MA0746.2 | chr16:31093244-31093257 | TGGGGGCGTGGTC | - | 6.16 | | SP4 | MA0685.1 | chr16:31093242-31093259 | CGTGGGGGCGTGGTCAG | - | 6.3 | | Stat6 | MA0520.1 | chr16:31093392-31093407 | GACTTCCAGAGAAAA | + | 6.17 | | ZEB1 | MA0103.3 | chr16:31094043-31094054 | GGGCAGGTGGG | - | 6.14 | | Zfx | MA0146.2 | chr16:31093256-31093270 | CAGGCCGAGGCTGC | - | 6.1 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CGGTAGGGGG CATGAAGGGT CCCAGGAGGA GGTGGGCACA CAGTGGAGGG GGAAGTCCAG 60
CCCCAAAGTC GGTGGGGGAG CAAGGAGTGA GAGGAGAGAG CCCCGGGGAT TCTAAGAGGT 120
GGGTGGGGGC TTGGCTATGG GGTGAGAGAA GTAGCTTGAG GATGTGCTGA GCTGAGCACC 180
CGCAAGTCAG GTATAACAAA TAGCAGGGTG GGTTGGGCAG CACGTGGGGG CGTGGTCAGG 240
CCGAGGCTGC TACCTGGGCT CCTCCATTAC ACTGTAGCCA GAATGGAATG GTCTTTCTGT 300
TCAGGGGAAG GTCACTGGGT ACCCCCTGGC TGCTGTGTCT GGAAACCCTC CTGAGTCAGC 360
CAGTAAAGTA ATGACTTCCA GAGAAAAAGA GGAAGCCATT GGTTTGGTCT AGGTTCCATT 420
CTTTCCTGGA GCAGGCCGGG TGCCAGGGAA CAAGGGATGG GGCATGGGCT CCACGGCTTC 480
CCTGCTGACT TGGCCACGGA AACTGGTTCA CTGGTTGGCA CCCTACTCCC TGTCCCTCTT 540
TCCCTGCGCC TTGTCTCTGC TGCTCCTCTC CTTGGAAACT AGACCTCTGG TCCTTCCCTG 600
TCAGTGTTGC TCCCATCTCT TCTCTAACCT TTATTCAGCC CCTTTTCCCT CTGCTGCCAA 660
CGGCCTTTTT AGGATCCAAC CAAACCACCC TTTCTACCTG CGCACCCTGC CACCCTCTGC 720
ACACCTTTAA CTGGAGGACT GAGTCACAGA TAATTGTTTC CTTGAAGTCC AGGCCCAGCT 780
GCAGCAACAA CAGTCATTAG CCCGTGTCAC ATCCCTGATC AGAGGGCATC TCCGTGGGGA 840
ATCGCCTCCA CCCAGCACTG CTGGAAGCCG CAGCTGCCAG GGAGTGGGGC GGCCGGTTCC 900
CTCAGCAGGA CCTGGGCTGG CCTCTCCACC TCCCCTAGTA GAGGCGGACC CATTCCATCT 960
AGTGGCCACC GAGGGTGGGT GGCCCTGAGA TGGTGGGCCC TTGACAGGCC TTGTCAGAGC 1020
AGAGGGCAGG TGGGAGTCAC CTGAAAGCTG AAGGAATGGC TTTAAGGATA GAAGATTTCT 1080
CATGACCTCA AGGGATATGA GGGAGGAGCC AGTTTGCCAG GGCTGGGAAA ATAATTAGGA 1140
GGCCTAGAAT CCCTGTTCTC ATCTGGGCCT CCGGGGCCAG GGGCAGGGGA ATGGCCTGCA 1200
GGGCTGGGAG GGGGTACACG CTGTGCGGGG TCTGCCCCTC AGTTGGTGAC CTCCTCTCTC 1260
TCTCCCCCCA 1270
|
| |
|
|
|
