| Tag | Content |
|---|
EnhancerAtlas ID | HS116-13107 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr16:8834090-8835310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GRHL1 | MA0647.1 | chr16:8835093-8835105 | CAAACCGGTTTT | + | 6.62 | | GRHL1 | MA0647.1 | chr16:8835093-8835105 | CAAACCGGTTTT | - | 6.74 | | Lhx3 | MA0135.1 | chr16:8835292-8835305 | AAATTAATTAACC | + | 7.22 | | MEF2A | MA0052.3 | chr16:8834919-8834931 | GCTAAAAATAGA | + | 6.92 | | MEF2B | MA0660.1 | chr16:8834919-8834931 | GCTAAAAATAGA | + | 6.44 | | MEF2C | MA0497.1 | chr16:8834917-8834932 | GAGCTAAAAATAGAC | + | 6.97 | | Stat4 | MA0518.1 | chr16:8835226-8835240 | CTTCTAGGAAACAG | + | 6.17 | | TFCP2 | MA0145.3 | chr16:8835094-8835104 | AAACCGGTTT | + | 6.02 | | TFCP2 | MA0145.3 | chr16:8835094-8835104 | AAACCGGTTT | - | 6.02 |
|
| | 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 |
| GH16I008740 | chr16 | 8833871 | 8836583 |
|
Enhancer Sequence | CATACCTCCA GATTTAGCAG ATTGGGATCC TATGTTTATT ATCTCACAGT TTCTGCGGGT 60
TGGGACTCCA GGGGTGACTT AGCCAGATCC TCTGGCTCAA GGTCTGTCAT GAGGGTGTAA 120
TGGAGCTGTC AGCTGGGGCT GTGGTCTCAT ATGATGGCTC AACTTGGCGG TTGGACGATC 180
TACTGGCAGT CCCACTTACG GGGTTGTGGC TGGATTCAGT TCCTTGGATG CTGTCAGCCA 240
GAAGCCACTC TCAGTTCCTT GATACGTGGA CCTCTTCACA GAGCCGCTTA CAATGTGGCA 300
ACTGCTCCCT CAAAGCAAGA GAGGGTGCCA AAAATGGAAG CCTCAGCCTG CAGCCATACC 360
CACAGCATTT TCCTGCTTCT CCATGGTGTC TCCACCAGGT CCCTGTGAGG CCATTAAAGT 420
GACGATAGTT AACGATCTGA CATGGTGTTC CCAATGGCAT CATTTTATGC CTCCCCAAAA 480
TTAATAATCT TATGTTGGTA AATAGAATAC AGAGAGTGGG AGACCACATC AAAATTGTTA 540
TTGCTGGGTA GAAAATTAAA TGTGTTTTCT TTTTTCCATG TTGCTTATTG GTATCTTCCT 600
CAATAAACAT TTTATCACAA AATAAGTGGG GTGGACAGTT GCAGGAGCAG ATAAAAAAAA 660
TTTTTTAACA GAAAAGCAGA GCAAACAACT CCAGTTGGAC TTGACCTTCG TTCTGGCCAG 720
GCTCATGTAC AGAGCTTTGG CTGTTTGGGA ACACGACATT CGTTTATCAC TCTCGGTCTA 780
AAGATCAAGA GAACATTAAC AATGTTTGCT AGCTACTGTG TAGTTTGGAG CTAAAAATAG 840
ACTCTGGCTT GGCATGGCCA TTGAGGGCTG TGAGCCCCAG AGGGCCAGGC TGGATGGACC 900
ATTCACATAT TGTGTCTGGT CTTGTGTGTC AATAACATAC TCTTGCCTTC TGGATGTGTT 960
ATTTTATTCA AGAATGAAAA TGCTTGATCA TTCAGTATTA ATTCAAACCG GTTTTTTGCA 1020
TCTTTGTGAT CATGATCAAA ATTTGCCTTT AGGAGAAGTG TGTTGTTTTG CTGCAAATGT 1080
TTCATTCAAA GGCTAGCACT CGATGAAATC AAAGATAGCC TCAGTTCCAT TCATAGCTTC 1140
TAGGAAACAG GTCAGATGGG CAAATTTCCT GCTAACCACT TGCTAGCTGT GTGATCTTGG 1200
GCAAATTAAT TAACCTCTCT 1220
|
