| Tag | Content |
|---|
EnhancerAtlas ID | HS147-34763 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr5:159860640-159861530 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MITF | MA0620.2 | chr5:159861375-159861393 | GCAGGTCACATGACTAAG | + | 6.16 | | MITF | MA0620.2 | chr5:159861375-159861393 | GCAGGTCACATGACTAAG | - | 6.16 | | RFX2 | MA0600.2 | chr5:159861181-159861197 | GGTTTCCATGGCAATG | - | 6.15 | | RFX2 | MA0600.2 | chr5:159861181-159861197 | GGTTTCCATGGCAATG | + | 6.18 | | RFX5 | MA0510.2 | chr5:159861181-159861197 | GGTTTCCATGGCAATG | + | 6.1 | | RFX5 | MA0510.2 | chr5:159861181-159861197 | GGTTTCCATGGCAATG | - | 6.24 |
|
| | 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 |
| GH05I160433 | chr5 | 159860458 | 159861424 |
|
Enhancer Sequence | AGAGGAACAC CTCTCCCACC ACGGACACAG CTTTTCTCTG CAGACATCCC CAAAGCGGGC 60
CACCTCATCT ATCAGGCCTC TTTCTGCTCC TGATGGTTGA TGCTCCTAGG ACTGGCATCT 120
CTTGGCAAGC CCAGAGCTAA CTTTAGAATA TGCTACACTC AGTGGCTTTT GGGGACTTTA 180
GCTGCATGTT TTCAAGCAAC AGGAACAATC AAACAGCAGA TCTGTCTCTC CTTTCCAGCC 240
AGAGTGAACT TGGACATGGG TCTTGTTTAT CCTTGCAGTC TCCAAGTCCA GTGTCTTGCC 300
TGGAGTAGAC GAATGATCAG TTTGTGGAAC TGAATCACGG CAGGAAGAAT GAGTGCAAAG 360
AGGCTCCCTT TGGCTCTGTG TGCACAGGCT CCTGGGAGGA TTTGTGCCTA CACTCCCTTC 420
TGAAGAGGCC TCTTTTTCCT ACAAGAGGAG CCTGGGACTG ATGAGCCATT TCTCTTTTCA 480
GATCACATAG TGGAACAGAC CGCAGGCCCC ACCTTCCTCC GCTGCCCGAG GAGTGGGAGT 540
GGGTTTCCAT GGCAATGGCA CGCACCAGCG CTCACCTCCG CTTTGCAGCC CTGCTGCAGA 600
GGTGAGAGCT GCCTGCCTTT GGTATGCTGC TCAGAGCCCA AGCCAGGCTG GCTCCTGGCT 660
TCCTGCAGTC TTGCAGGGAG GGACACCAGA AAGGACAGCA GTGTAGGGAC GCTAGCCCAG 720
AGGTATAAGT CAGGGGCAGG TCACATGACT AAGAAGCATC TTCATCTTAC TGGAAAGATG 780
AAAAGTTAGT TGAGTATGAT GTTCTGTATT ACTAGTTGGA AAACTGGGCA TGTGACTAGA 840
GCCGTACAAC ACATCGTATT TCAGTCTTGT AGTTGGAGGC AGAGAGGGTG 890
|
