| Tag | Content |
|---|
EnhancerAtlas ID | HS136-16533 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr6:10889180-10890510 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr6:10890023-10890035 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr6:10890023-10890035 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr6:10890022-10890037 | TTCTATTTTTAGTAG | - | 6.57 | | SPI1 | MA0080.4 | chr6:10889797-10889811 | CACTTCCTCTTTTC | - | 6.92 |
|
| | 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 |
| GH06I010889 | chr6 | 10889525 | 10890233 |
|
Enhancer Sequence | ACCTCCTGGG TTCGAGTGAT TCTCCTTCCT CAGCCTCACG AGTAGCTGGG TCTACAGTCA 60
CGTGCCACTG CGCCCAGCTA ATTTTTGTAT TTTTTAGTAG AGACGGGTTT CACCATATTG 120
GACAGGCTGG TCTCGAACTC CTGACCTCAT GATATGCCCG CCTTGGCCTC CCAAAGTGCT 180
GGGATTACAG GCGTGAGCCA CTGCGCCTGG CCTAACACCC AATTTTAATT GTAGCTTTAG 240
CTGTTCCTCC TATCTCACTT TTGCCTCTAC TCAATTATCC ACTAACACAA TGGTTCTTTT 300
TCTTTGCCTT TATCATTTAT TTTTAATTGA CACATATATT AATTGACACA TAGTAATTGC 360
ACATGTTAAT TGGGTGTAGT GTGATATTTC CATATGTGTA TACAGTGTGT AATGATCAAA 420
TCAGGGTAAT TATGCATATC CATCACCTCA AATATTTATT TCTTTGTGTT GGGAATGTTC 480
AAAATCTACT CGTATAGCTA TTTGAAAATA TACAATAAGT TGTACATTAT AGTCACCTTG 540
CAGTACTATC TTACTCTAGA ACTTACTCCT TCCAGCTAGC TGTAATTTTG TGTTCATTAA 600
CTAACCTCTG CCTATCTCAC TTCCTCTTTT CTAGTGACCA CTATTCTCTC TACTTCTATG 660
AGATCAGCCT TTTTTTTTTT TTTTTTTTTT GAGATGGAGT TTCACTCTTG CTTCCCCAGC 720
TGGAGTGCAA TAGTGCAACC TTAGCTCATT GCAACCTCCG CGTCCCGGGT TCAAGCGATT 780
CTCTTGCTTC AGCCTCCCCC GTAGCTGGGA TTACAGGCAT GCGCCACCCT GCCCGGATAA 840
TTTTCTATTT TTAGTAGAGA CAGGGTTTTG TCATGTTGGC CAGGCTGGTC TCCAACTCCT 900
GACCTCAGGT GATCCACCCA CCTCGGCCAC CCAAAGTGCT GGGATTACAG GCATGAGCCA 960
CCGCACCCGG CCGAGATCAG CTTTTTTAGC CTCTACATGT GATCAAGAAC ATGCAGTGTG 1020
TCTGTCTGTG CCCCGCTTAT TTCATTTAGC ATAATGTCCT TCAGGCTCAT GCATGTTACC 1080
ATGAATGACA GGATTTTGTT CTTTTTTCTG GCTGAAAAGT ATTCCACTGT GTGAATATAC 1140
CACATTTTCT TTATCCATTC ATCCACTGAT GGACACTTAA GTTGATTCCA TATCTTGGCT 1200
ATTATGAATA GCGCTGCAGT AAACATGGGA GTGCAGATAT GCCTTTGACA TACTGATTTC 1260
TTTTCTTTTG GATATATCTC CAGGAGTGGA ATTGCTGGAT TTATGATAGT TTTTTGAGGA 1320
ACCTCCATAC 1330
|
