| Tag | Content |
|---|
EnhancerAtlas ID | HS062-09067 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr2:65243810-65245200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF9 | MA0653.1 | chr2:65244135-65244150 | GGTTTCTGTTTCATT | - | 6.06 | | ZNF263 | MA0528.1 | chr2:65244177-65244198 | TCTTCTCCCTCTTGCTCCTTA | - | 6.37 | | ZNF263 | MA0528.1 | chr2:65244174-65244195 | TTCTCTTCTCCCTCTTGCTCC | - | 6.75 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 65244028 | 65244159 | | chr2 | 65244534 | 65244958 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I065016 | chr2 | 65243935 | 65247080 |
|
Enhancer Sequence | AGTGGGTTTT GGGTCTCTTC ACTGCTCTGA GCCATGTTAA CATGGAACCA GGTGAGCCCA 60
GTGGTAGATG CACAACCAGT GTCTTGACAT ACTTTAATTC CTGGAAAACT CTAAATCGGT 120
CTTCTGTTAT TTTTTTGTTT TTTCTTCTTT AAGAGACAGG ATCTTCCCGT GATTGCCCAG 180
GCTGGTCTCG AACTCCTGGG CTCAAGTGAT CCTCCCACCT CGGCCTTCCG AATAGCTGTG 240
ATTACAGGCA TGCACAGCCA CACCAAGCCT CACATGATTT CTTAAAATGA CCAGCCCCAA 300
AGCTTTTCTG TATTCCCCTG GGGTGGGTTT CTGTTTCATT TACTATTCTA CTGAAGTTAC 360
CTCATTCTCT TCTCCCTCTT GCTCCTTAGA GGTCAGCAGA TCATTAGTTA GCCCAGCTGC 420
GGGTCCCTCA CCCTAATTAG GAAGACCTTT CCCTGAGTAA AAGAAGGCAG CCCACCTAAC 480
TCAAAAATGC ATTGCAGGGA AGTTTCTAGA ATGGTTCCTG CCCAATTCTC CCTTTCTGGA 540
TATGTGAATT AGAAAACGAG TCTGAGGCAC CGTGGTGAGG GATGGATGCT TAGCCCTCTA 600
GGAGTCCACA ATAGTGTGGG ATTGTCTCAT TTGGCACAAG AGATGCATCC TGTCATTCAC 660
TGGAAAACCT TAAAAAAAAA AAAAAACACT GGGTTTTCCA AATATGTTAA AACTTTCAAA 720
GGACGGCAGC ACGTCGTTTC ATTCACACAT TTAGTTTTGC CTCTACTGCT CACTTCCTCC 780
CAATCTGGAT GGCTATTTAT ATAACACAGA GGTGGGAGTA AAAAAAAAAA AAAAATTAGG 840
GAAGGAAGTT CCTCTGGCCT AGACAAAAAC CTGTTTCTCA GCTGCACCAA CTAACCTCTG 900
CAGAGCCCGC AGAGCCAGCT AGAGGGAGCA GGTACTGTTC TTATGGTTAT CTACTTAGTT 960
ATTCTTCCAA GCTCACAGAG CCATTTCTGG GTTTTGGCCT AAAAGAAAAA AAAATCATAG 1020
TTTACCATTT ACTTTTGGGA GGGGAACACT CAAGAGAGGA GATGCACATG TAGAGAAACT 1080
AGTTGTTTGT TCTCTCGGGA ACGTTTTGCA CCGGGAGGCA ATGTGCAGTT CTTAAGAAAC 1140
TTGGAACACG TGAATCCAAG TAAATGACAG AATAGGTAAA TGAAGGCAGT CATATTTTAA 1200
GTATCTTGGG AGTTGCCAAA GCCTCATGTT GTGACAGAAG TTTTAAAGTG ATTCTGTTTT 1260
TTCCCTTATT TCAAGAGAAG AAAGCCAGAA ACGAAGATGG TGCTAATTGC TCTGTTCTGG 1320
GGTCTGAGAC AAGACACATG TTAGCCTGCC TCGGACTGTT GTCATGTCTG GCGGTTTGTT 1380
TTTCCCATTT 1390
|
