| Tag | Content |
|---|
EnhancerAtlas ID | HS060-29254 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr6:24743420-24744580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr6:24744308-24744319 | CTAATCCTCTT | - | 6.62 | | JUN(var.2) | MA0489.1 | chr6:24743642-24743656 | AAGATATGAGTCAT | + | 6.21 | | YY1 | MA0095.2 | chr6:24743762-24743774 | CAAAATGGCTGC | + | 6.52 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 24743523 | 24743742 | | chr6 | 24743891 | 24744276 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I024742 | chr6 | 24742463 | 24745084 |
|
Enhancer Sequence | ACAAGCTGAA CATTAAGGTC ATTGATATCA TCTGAAGCCA GGAAGAGTCT CTGCTAGGAA 60
GACTTTTAGC ACAAAATCAA CTATTCTCTG CTCCAAGTAA AATGTCTAAA CTGTCTGCAA 120
AGGCAAATGG CTAAAAGCTT TGACAGGAAT ACTTCGTTAA GTGAGATTAG TCATGACCTC 180
TTAGTAATAT AAGCCTGAAG AAAGAAATGA AAGTTGGAAG TAAAGATATG AGTCATGCTG 240
CAACTTGGTA GCTGGCATTC ATTCAGGAGC TCAACAATGT CAGCAGATCT TAGGCTCCTT 300
CCTTCTGCTC TGCCAGTCCT TATTCTTGTT AACTCATAAA TTCAAAATGG CTGCCACAGC 360
TCCCAACATC ACAGTTCAAA GGCAGAAAAC AGGGTAGTCA GGGTAAAAGT CTTTATCCTT 420
CTGGGGCTAC TCTTATCAGG CGAAAGATTA CCTTTCCCAG TAGCCCTGTA GTAGACTTCC 480
CCTCAAATCT CTTTGCCATA TAACTGACTA CTCTTAGATG TAAGGAAGGC TGACAGAAGG 540
ACACAGAATG GCTATGACTG GCTTAGCTAA TAATGACTCA TCTGCTAGGG CTGGGTACAT 600
TCCCCAGACA AAATAAGGCA GTGGGGCAGG AGCAGGGAAA TGGCTGTTGA GTAAGCAACA 660
GTGTCTGTCA CAGTGAATTT AGCCCATATA CATATAAGTT TGGTCTTAAT TCTGTATCAA 720
ATTTTGTATG ATATTTTCTG GGTTTTTGTT GTTGTTGTTA CTTTTTGAAC ACTTCTCTAC 780
TGGACTGTAT TTTCTTTGTG TTTGCATGTG TGTGTTTCCT AATAGTTTAT AGGGAAATAA 840
ATTTTTGTTC TAGTGGTTAC CTTATAACTA CAAGTTTATA TAATAAACCT AATCCTCTTT 900
CTTCAAGCAA AACCAGTTGA CTCCATACTA TGAACACTGA CAAAATTAGC ACACTATCAC 960
TTCCCTTTTT CTGCTGTTCT TAGTATTTAT CTTCGCTTTT TTTTTTTTTT TTTTTTTTGT 1020
AGAGACATGG TTTCACCATG TTGGCCAGGC TGGTCTTGAA CTCCTGGCCT CAAGTGATCC 1080
ACCCACTTAG GCCTCCCAAA GTGCTAGGAT TATAGGCGTG AACCACCACG CCTGGCCTTT 1140
ATCTTTGCGT TTCTAAATAT 1160
|
