| Tag | Content |
|---|
EnhancerAtlas ID | HS116-11701 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr15:42970530-42971940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROD2 | MA0668.1 | chr15:42971884-42971894 | GCCATATGGT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr15 | 42971410 | 42971764 | | chr15 | 42970670 | 42970996 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH15I042679 | chr15 | 42971601 | 42971750 | | GH15I042680 | chr15 | 42971772 | 42972614 |
|
Enhancer Sequence | TTCCCTCATT TATCTCTGGA GCAGCATTCA TGAGGAGCCT GCAAAGCTGG AGCTAGCTCC 60
AGAGCCAGGG GAAATTGGCC AGTCTGCCTT CCTTTTCTCC TTGCAGCAGT AATCTGGACC 120
AGAGGGGAAT TTGTCTTTGA ATACCATTGC CTGTGTTCTT GGCATTTTCC CATTTGGAAT 180
TGTAGGGGGT TAACCTTAAG TGCCTAGAGC CTGGGAGACA CTGTTGCTGC TTCCGCTGCC 240
ACCACCGCTG CCACTGCGGC TTTAGTAAGT AGATGCCACT GCAATCTGCT GCAGAAGCTG 300
CCAGACCCCG AGGCTGGGGG ACAGCTGTGA GAGAAGAAGC AGGAGAGTGC AGTGGAGTCC 360
TCACAAGCAG GTGTCTAGGC AGCAGCTGGG GGATACTGGA GCCATCAGAG ATGAAGGGCA 420
ATTACCTGAT AAAGACAGAG GTCCCTTGGC TGGCAGGTAA ATGAAGACTT GCCCTTTGTA 480
ATCTAGCCAG ACATGTAGTA TAAGGTTGCT ATTTTCTTTT TCACCTGCTT TCTGGGAACT 540
TGACAAAATG TGCTTAGCAG AGGGACCATT CTGTGCGGCC TCTTGGGTGA ATGTGCTGCA 600
TCTATACAGA TGGCAGCAGA CAGCCTCTCC TTGCAGGTCC TATGGCTATG CAGGAAACAA 660
TATCATAGCT GTCACTTTCT TAGGTGAAGG GTAAGGAGCA CCCCTTCTAG GGAGAAGCAG 720
ATTGTAAATC TGAAGGTTGA GGAGAAAGCC AGACAAGGAG ACTGAGTAAT CTCAGGGAGT 780
TCAGATAAAG ACCCTGTCTC AGCCTCTTGC ATCTGGTGGT CTGTGGGTCT TAGCTGGGTT 840
TGTCTAGGAT GGGCTCATGT TTGTAATTCA GCCATTTCTA TAGTCAGACA AAATTTGGAG 900
CAGTAATACA AGCATGATAC ATATGGATGT ATGTTTCCTG TTAACTGCTT TCTCTATTTG 960
TTTGGCATTA ACAGGTTTCT ATTCCAGTTG CTATCCTGAG CCTCCACATA ACAGAGAGTA 1020
ACCTTCCTCT TTCTGTATGC TCCACTGTGT ATATTTGGCC TTTTGCCCAC AGCAATCAGT 1080
GCCAGTCTTT TGAGCACACT CACTCAAGTG TCTGGACCTG TCCTAGTCCT TGGACCTGTT 1140
GCAGATTGAA TGACCTCATA GCCTTCTTCC CTGGGAAGAG ACTGTGGTTG TGTCAGCTCC 1200
CACTCCCATT CCCCCGGGCT ATTCCACCTA TCACTCTTCA CCCATCCATC TTTTACTATC 1260
CTCCAAAGGC TGCGTTATGA AATCTTAATT TCTTCCAAGG CAGGGGCGGC AAACATTTTC 1320
TGTAAAAGGC CAGATAGTAT TTTAGGCTTT GTGGGCCATA TGGTCTGTGC TGCAACTACT 1380
CAATTTTGCC AGGGTGGTGC AAAAGCAGCC 1410
|
