| Tag | Content |
|---|
EnhancerAtlas ID | HS095-25099 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr5:159860410-159861650 |
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 | CTCCCCGCAG TGCAGTGAGA AGGCTGAAAA GGACAATAAA TACTCCCAGA ATGCTCTCTC 60
AAGAGCCCTC TCTCTCACCA GTCTTGGTTC TGTTGGTGGC ACCAGCATAG GCTTACCTAT 120
TTCTCCTGCA ACTCAGCTGG TGTGTGTCTG GGGGTGAGAG GCCATTCTCC CCTTCCTGAA 180
GATTCCTATC TTTATGTGTT CATTTAAAGC TTTTCATGAC TGCAGGTAGG AGAGGAACAC 240
CTCTCCCACC ACGGACACAG CTTTTCTCTG CAGACATCCC CAAAGCGGGC CACCTCATCT 300
ATCAGGCCTC TTTCTGCTCC TGATGGTTGA TGCTCCTAGG ACTGGCATCT CTTGGCAAGC 360
CCAGAGCTAA CTTTAGAATA TGCTACACTC AGTGGCTTTT GGGGACTTTA GCTGCATGTT 420
TTCAAGCAAC AGGAACAATC AAACAGCAGA TCTGTCTCTC CTTTCCAGCC AGAGTGAACT 480
TGGACATGGG TCTTGTTTAT CCTTGCAGTC TCCAAGTCCA GTGTCTTGCC TGGAGTAGAC 540
GAATGATCAG TTTGTGGAAC TGAATCACGG CAGGAAGAAT GAGTGCAAAG AGGCTCCCTT 600
TGGCTCTGTG TGCACAGGCT CCTGGGAGGA TTTGTGCCTA CACTCCCTTC TGAAGAGGCC 660
TCTTTTTCCT ACAAGAGGAG CCTGGGACTG ATGAGCCATT TCTCTTTTCA GATCACATAG 720
TGGAACAGAC CGCAGGCCCC ACCTTCCTCC GCTGCCCGAG GAGTGGGAGT GGGTTTCCAT 780
GGCAATGGCA CGCACCAGCG CTCACCTCCG CTTTGCAGCC CTGCTGCAGA GGTGAGAGCT 840
GCCTGCCTTT GGTATGCTGC TCAGAGCCCA AGCCAGGCTG GCTCCTGGCT TCCTGCAGTC 900
TTGCAGGGAG GGACACCAGA AAGGACAGCA GTGTAGGGAC GCTAGCCCAG AGGTATAAGT 960
CAGGGGCAGG TCACATGACT AAGAAGCATC TTCATCTTAC TGGAAAGATG AAAAGTTAGT 1020
TGAGTATGAT GTTCTGTATT ACTAGTTGGA AAACTGGGCA TGTGACTAGA GCCGTACAAC 1080
ACATCGTATT TCAGTCTTGT AGTTGGAGGC AGAGAGGGTG GTATGTGAGA TGCCACAGGG 1140
GAGAGAGGGA AAGGCAGGCA TGGACTCATA CCTTGAAAAA GAGACAGAGA AAGAAGGGGG 1200
ACCTAAGAAA GCAGCAGACA CAAAACTACA TGGTGCTTGG 1240
|
