| Tag | Content |
|---|
EnhancerAtlas ID | HS095-29838 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr8:101818780-101819850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF143 | MA0088.2 | chr8:101819802-101819818 | TTCCCATAATCCCTTG | + | 6.06 | | ZNF263 | MA0528.1 | chr8:101819372-101819393 | CATCCCATCCCCTCCTCCTTC | - | 6.53 |
|
| | 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 |
| GH08I100806 | chr8 | 101818921 | 101819794 |
|
Enhancer Sequence | GCACATATAT GCAGGCATGC ATGCACGCAT GTACCACTAG AGTGTAAAGT ATCTTTTGGC 60
CCAGTCCCTT AGGTCACCTG AAATGCTTCT AGTTCACAGG TGCTGTGAGC GGGTCACATT 120
CTAGTAGTGG TGCTCTAGGG TGGTTCTAGG GCCATCTTTG CTGAAAGAGC AGGACACATG 180
GGTATTGGGC ACCTGCTTTT CCTCCCCCAG AGCAGCTGGG AAGTGCTAGA TTGTCCTTGT 240
GAGAGTCTGA CCTTGCCTTG GAGCAAAGAG AGATGAGAGG CTCCCAAAAC ACCATGGGAG 300
TGTGTGCGTG TGTGTGTGTG TATATGTGTG TGCGCGCGCA CGCACAGGGC TATTTGGTGC 360
TTGGAAAGAT TGAGCCTCAG CCTTCTGGAA TGCATGTCCT ACTGAGGACT TCTAGCTCTT 420
CCTGGATCCT TATATGCCCA TTTGCTATTG TAAATAGCTA TATGACGTTG TGATACTATT 480
CCAAACCCTA GTCATAGCAA CCACATACCT AATAGCCAAG GGATAACCAT ACTATCTTCC 540
CTTTCTGAAG AACCTTTCAG CAAAAGATTT CAGGGAATTT TACCAAGAAA ACCATCCCAT 600
CCCCTCCTCC TTCCATTTGA CAGGTGGAGA AGTGAGGCAC AGTGAAGCCA GAGGAGCCTG 660
GTCAGACGGT GAGTCAGAAG TAGAGCAGGG CTGCACCTGG TGACACCTAT TTCCTCCCTT 720
GTGGTTTGGC CCCTGCCTCA TAGGCTTCCT GGAAAGGTGT AGCTTCTTCA TGGCTTACTT 780
GTTGAGTAAA CACTGCTATG AGCTTTCAAA TATTTCCCTA GGTTGCAGGA GGTTGTGTCT 840
CTCAGCAAAA AGTAAGTGTT GAGGCTGAGC ACAATGGCTC GCACCTGTTA TCCCAGGCCT 900
TTGGGAGGCC AAGGCAGGAG GATCACTTGA GCCCAGGAGA TTGAGACCAG CCTGGGCAAC 960
ATGGTGAAAC CCTGTGATAT GGTTTGGCTG TGTCCCCACC CAAATCTCAT CTTGAATTGT 1020
AGTTCCCATA ATCCCTTGGT ATTATGGAAG GGACCAGGTG GAGATAATTG 1070
|
