| Tag | Content |
|---|
EnhancerAtlas ID | HS197-10223 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr19:5563560-5564720 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EHF | MA0598.2 | chr19:5564179-5564191 | TACCCGGAAGTG | + | 6.37 | | ELF1 | MA0473.2 | chr19:5564179-5564191 | TACCCGGAAGTG | + | 6.62 | | ELF3 | MA0640.1 | chr19:5564179-5564192 | TACCCGGAAGTGA | + | 7.04 | | ELF4 | MA0641.1 | chr19:5564179-5564191 | TACCCGGAAGTG | + | 6.74 | | ELF5 | MA0136.2 | chr19:5564180-5564191 | ACCCGGAAGTG | + | 6.32 | | ZBTB7A | MA0750.2 | chr19:5564180-5564193 | ACCCGGAAGTGAG | + | 6.15 | | ZNF263 | MA0528.1 | chr19:5564152-5564173 | GGGGGAGGGAGAAGAGGGGGC | + | 7.44 |
|
| | 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 |
| GH19I005563 | chr19 | 5563052 | 5565360 |
|
Enhancer Sequence | AGACCCTGGC TCTGCCCCTT CCCAGCTTAA TCTTACTCTG CCTCAGCTTC TCCACCTGTA 60
AACCGCCAAT GATAACGGCA CCCGGCCAGG CACGGTGGCT CACGCGTGTA ATCCCAGCAC 120
TTTGGGAGGC TGAGGTAGGC AGATCACCTG AGGTTAGGAG TTTGAGACCA GCCTGGCCAA 180
CATGGTGAAA CGGTCTCTAC TAAAAATACA AAAAAATTAG CCAGGCATGG TGGCGGGCGC 240
CTGTAATCCC AGCTACTCAG GAGACTGAGG CAGGAGAATC GCTTGAACCC GGGAGGCAGA 300
GGTTGCAGTG AGCCGAGATT GCGCCACTGC ACTCCAGCCT GGGCGACAGA GCAAGACTCC 360
CGTCTCAAAA ATAATAAATA ATAAATAAAT AAAAGCATCC TCGCCAGGGG ACAGCGGTAA 420
GGCCACGTGA AAAGCCCCTA GCATCTCAAA GGCTCTCAAA GCATGACCAT GACTCAGTGC 480
CTGCTAGCTC CCGTGACAAC CTGTCTCCCT GCAACGCTGC TGCCTCGAGG CAGAAAATGT 540
TGTCACTACT GCATTTCACA GAGTGTAGAA ACAGGAGGTG GCAAGAGAGG CTGGGGGAGG 600
GAGAAGAGGG GGCCCTATCT ACCCGGAAGT GAGAGAGGGC CTGGCAGGTT TGTCCCGAGC 660
AGCCCACGCA GCTTCTCTCT CCCTAGGGTA CCGTCTGCGC TGACAGGTCC CAAGTGTTTT 720
TCTCATTTCT CACATGGGGA AGCTGAGGCC TCCCCGGCTG CTGCTGCACC ATCCACTAGT 780
AGCCCCTGCT CTGCCTCTAG AGGTCTGGGA GTGGTCTGGG GAGCTCAGAA CCCATTTGAT 840
GCCCAGAGAG GGTGGGTTAG CTGCCTCGGG ACACACAGCC AGTGAACAGC AAAGGCAGAT 900
AGGGGCCCCT GTCTGTTGGG GAAGACAAAG CTGGACTCTG CCATCAACCC CAGCTGTGTG 960
TGTGGTCAGG GATGGGCAAG GGGCAGGGCA TTAGGACAGG GTGGGAGCCC AGAGGAGGTT 1020
GAAACTCTCT CTTTTTTCTT TTGTTTTGAG ACGGAGTCTC ACTCTGTTGT CCAGGCTGGA 1080
GTGCAGAGGC ACGATCTCAG CTCACTGCAA CCTCCGCCTC CAGGTTCAAG CGATTCTCCT 1140
GCCTCAGCCT CCCAAGTAGC 1160
|
