| Tag | Content |
|---|
EnhancerAtlas ID | HS099-19694 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr6:111844070-111845450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr6:111844282-111844294 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr6:111844286-111844298 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr6:111844290-111844302 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr6:111844294-111844306 | GTTTGTTTGTTT | + | 6.32 |
|
| | 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 |
| GH06I111523 | chr6 | 111844804 | 111845203 |
|
Enhancer Sequence | TTAGGTTCTC CTTCTTTGTA TATCAGTCGA TAGAGTGCCT CCAGGCAGAA GGCTGGAACT 60
CAGTTCATTT TTCTTTCCCA AGGGATCACA GTCCTCCTGT ACTACCTGTT GTTCAGATTT 120
TCAAAGCGGT TACTTTATAT ATTTTGTCTA CTTTTACTAT TTTTTATAGC AGATGCTAGT 180
CCCATATTAG TTACTCCATC ATTGATTCTT TTGTTTGTTT GTTTGTTTGT TTGTTTTTTA 240
AACAGAGTCT GGCTGTCACC AGGCTGGAGT GCAGTGGCGA GATCTCGGCT CACTGAAACC 300
TCCGCCTCCT AGGTTCAAGC GACTCTCCTG CCTCAGCCTC CCTAGTAGCT GGGACTACAG 360
GCATGTGCCA CCACGCCCAG CTAATTTTTG TATTTTTAGT AGAGATGGTG TTTCACCACG 420
ATGTCCAGGA TGGTCTCAAT CTCCTGGCCT CATGATCCGC CTGCCTTGGC CTCGCAAAGT 480
GCTGGGATTA CAGGCGTGAG CCACCGTGCC CGGCCTGATT CTGTCTTTTT AGCATTTACT 540
TCTTTATAAG TTTTAGGATT TTGATTAGCA TAATCACTTT GAGTGGGAGA TATTTTTGTT 600
GTCACCCTTT CTTGGCCTGT CTCCAAGTTT GATGAATATT TCTATCTGCC CTTTTCCTCA 660
TTCCATATCC CAGTCCAGAG CCAGTTCTTA AAATGGCTTT AGAGGGCTCC TACTCCTTAC 720
TGATATCCGG AATATGGCCA ATTCAGTAAC TGAACCAGCT GTTAGCTCAG CTCAGTTGCT 780
GTAGTGATGT TTTTCTTTTG TCATTTTGCC CTCTTGGGTC CAAAGCTTCC CATAAATGCA 840
CAGCCCCAGG CAGAATCAGA AGCAGTTTAA TTTAGCCTCC TTTCATGAGA CTGGGGAAAA 900
CCAGGTGACA AACCACTGTT TGCCTGGAAC TAAAGGGTTT CTTGGGATTT GGGATGATCA 960
GTGCTAAAAC AGGAAGAGTC CTAGGAAAAC CAGGAAGGCT GATCACCTCA GTCATGCCCC 1020
AGTTTCTGGC TTCCAGTAAC ATGGCTGGCA TTGGTCTTCA TCTTTAGCAG AGCATTTTAG 1080
TCTGTGTATT CCACAAGAGC TGAGTTTCCA GTTGCCACTA GCTGCCTCAA GACCCAGACC 1140
CTGATCGACT ACAGCTCTAG CCCAGCTTAC TGCTTTGCAT TTCTATTGTG TTTCTGGTCC 1200
ACAAAGATGT TAGTTTTGTT TTTTAAACCC AACAATGGCC TTTTAGTTTT CTTTTTTTCT 1260
GTTTTATCTC TCATTACCAT GTGTTTAGAG CATATAAGAT AAGCTGAAAC ATGAATTTAC 1320
TGTGCCACCT TGTTTGGAAA TTCTACTGAT TCTTTTTCAA TTTGATATTG TCTTGGCTTA 1380
|
