| Tag | Content |
|---|
EnhancerAtlas ID | HS147-03195 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:151568640-151569880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HLF | MA0043.2 | chr1:151569688-151569700 | GGTTATGTAATG | - | 6.62 | | MAFF | MA0495.3 | chr1:151568769-151568784 | TTGCTTACTCAGCAG | + | 6.53 | | MAFF | MA0495.3 | chr1:151568769-151568784 | TTGCTTACTCAGCAG | - | 6.5 | | MAFG | MA0659.1 | chr1:151568766-151568787 | GTGTTGCTTACTCAGCAGCAA | - | 6.03 | | MAFK | MA0496.2 | chr1:151568767-151568786 | TGTTGCTTACTCAGCAGCA | + | 6.09 | | MAFK | MA0496.2 | chr1:151568767-151568786 | TGTTGCTTACTCAGCAGCA | - | 6.36 |
|
| | 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 |
| GH01I151596 | chr1 | 151568601 | 151569513 |
|
Enhancer Sequence | TTTCCAAATG TAGAAGGCCT GGATCCCTTG AGAAGACAGT TCTCACTAGC AGATTATAAT 60
CTTGTAGAAG ATCTAGAACA CTCATGGAAC AAAGAGTTAA GGATATCATC TTCATCTAGA 120
AAAATAGTGT TGCTTACTCA GCAGCAATAG GACTAGAACT TCAATTTGTT TTTGCCTTCC 180
TTCTCCCTGG GCCACGGAGG GGTCATGGTC GGGATTAAGC TGCCTGTGGC TTTACTCGTT 240
CAGTCTCATT TCTGGACCTC TGCTACCTTG CCAGTTGTTT CTGAGACACA CCATGTCCTT 300
CTTCACCTCT CTGCCTTTCC ATGTGTGCTT CCTTCGGCCT GAAATTCTTT TCCCTGCCTT 360
ATCCTTCTGA GAAGCTCCTA GTCATCCTTC AAAACCCCAC TCAAATGACA TCTGTTTGGT 420
GAAGTCTTCT CTGACTCCCC AGAGAATCCC CAGACAGAGT TAATCATCCC TTATCAGGGC 480
TCCCACAGCA GCTGGCACAA AACTTATCAC AATGTACACT ACTTGTTTGT TTTCATGTCT 540
GCCTCTCCCC CAGGCCTGAG AATTCCTAAG GGAAGGGGTT GATTATTCAT CTTCATGTCT 600
GCAGCCCTGG CCCAGTGCCT GGCAGGTAGT AGGGACCCAG TCAGTGCTGG CAGAACTGAA 660
GTAAGTTCTC CTTCCTGTAA CCAGCAGAGT GTTTTTCCAG GTGGCTGACC AGGATCACTG 720
AGCAAAAGAC AATCACTCCA TGAGGCAGCC CTGGGGCACT TGCCTGGCAT CAGGAGCTCA 780
ACGCAGAGAA CTGAATGCTA ATGTTTAATG TTTGTGCACT GGAGGGCACA CATCATTCAA 840
AATTTGATGG AGGCTGTTTA GAATCTATTT TAATCCCAGA AGATGACATG TAAGGAGAAA 900
TTTTCTGATA GTGTGATTAA GCTCTGGGAC ATGAGTTAAA GGGGTGGTGG GTGTTGCAAT 960
GTTGAAGGTC TTTATAGTCT CTGATTTTTT CAGAAAAGAC TGTGTGGAGT GAGTAGCTGA 1020
AATGTGAATA GATGACCTCT GATTTTAAGG TTATGTAATG GGATTGGATA GGTCTCTTGC 1080
TCGCTCTGGG CATTGGACAT GGTGTGGGGC TTTGGTAGCT TCAGGTGGAA TGACCTGGCC 1140
CTCCATGAAT GAGTGTTGAG GTTGGACACA CGGCTGCCAC TTCTCTGTAC TGCTCCCCAC 1200
AGCTTAGCCT CATCTGCAAA CTTCGGAGGG ATCAGTCCAT 1240
|
