Tag | Content |
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EnhancerAtlas ID | HS116-19051 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr2:102854620-102855650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB3 | MA0638.1 | chr2:102854992-102855006 | CTGCCACGTCATGG | + | 6.23 | TEAD1 | MA0090.2 | chr2:102854915-102854925 | ATGGAATGTG | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 102854878 | 102855173 | chr2 | 102854655 | 102855173 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I102238 | chr2 | 102854507 | 102858977 |
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Enhancer Sequence | GCTGCGAGCG GAGATTGGAC CAGAGAGGTG AAATACAGGT GCTGAGTCGC TGGGTTACCT 60 TTACATTCAC CTTCCCATAA TGACTGAGTC AGCCACAAAA CCCACTACCT TTGGTATCTC 120 CCCTCAAATA CCCTGAGTCG GCTCATGAGA GAGGCCCTGG GAAAGACCCA GTCACATTAA 180 ATAAAGGGAC CGGGAAGGTG TGGTCTTTCC CCGGAGGACC AAGCAAGATG AAGATATACA 240 TGTGAAAAGT GCTTGGCAAA CCGTGGGATG CCATGAGGAG CTGGCCTGCC AAAATATGGA 300 ATGTGCTCAG GGAGCCTCAG TCCCCAGGGC CCCCCACACC CATCAGCACC CCATAGTGAC 360 GCAGACCACT TCCTGCCACG TCATGGTTGG TTGACCTTTC CTCGGCACTT GGTCCTGTTT 420 TTTATTTATA AACTTCCCTC TAACACATGC TTGTTTGGTA TTGATCTGGG GCTGTGTAAA 480 GTGGAAAATT CCTTCCTGGT TTCCTTGAAG AACAGAGGCT GTTCCAGATG AGGTCTGGAG 540 TGAGCTACAG AGGGTGATGC TGGCTTTAGG AGTGGTGGCT GCTGGGTCTG AATGTTAGAG 600 GCCACACATC TCCAGTAGTA ATATTATTCT GGGAGATGGG AACTCTGTGT GTGGATGTCC 660 CCTCCCATAC ACCCAGGAAC TTCTGAGAAA TGCTGCTGTT CACTAATACA ATTCCACCCT 720 CATCTCCCAG GCTGTCCCTG GAGAGGAGCT CTCCACTTGA GAAGGACCTC AGAGCCCTGG 780 CTCTTGTCAT CCAAATTCAC CTTTCCTCTG GGGCTCTTAT AGGAAAGGTG AGAGTTGACA 840 CTGCTCACCT GTGATCCTCT GGCATAACCA CCTTGCAAAG ATAACCCAAG AGAAATGGAA 900 GCCTCAGGGA TATACCACCA GATGAACTGA CGGCAAGGTG GAGGTTTTCG CATTCCCATG 960 GCAGGTTTCC TTATCAGCCC CCATCTCCCA CCACATCAGA AAAGGAGTAA ATAGATCTTT 1020 CCTGATTTCA 1030
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