| Tag | Content |
|---|
EnhancerAtlas ID | HS043-13533 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr14:75400270-75402470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr14:75402058-75402071 | GGAAACAGCTGCT | - | 6.14 | | Myod1 | MA0499.1 | chr14:75400826-75400839 | TGCAGCTGTTGCC | + | 6.41 | | Tcf12 | MA0521.1 | chr14:75402061-75402072 | AACAGCTGCTG | + | 6.32 | | ZNF263 | MA0528.1 | chr14:75402266-75402287 | CCTTCTCTCTCTCCATCCTCA | - | 6.18 | | ZNF263 | MA0528.1 | chr14:75401016-75401037 | GGGGGAAGAAGGGGAAGGGCA | + | 6.19 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 75401816 | 75402439 | | chr14 | 75401325 | 75401806 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I074931 | chr14 | 75398458 | 75402558 |
|
Enhancer Sequence | TCTCCTTCAT CTGTTCCTTT CTTCCCTGTC TTCATCCTTG GTGGTGATGG TGGTAGTGGG 60
GTCTTTGGAT ATAATGCACC ATAATAAAAA TTATGCCAAG AGATGTGATC CACTTTATCA 120
AAAAGGAAAT GTATTTGTTT TGTAGGTGCT CCACGTGGGG ACACACGAGG GTCCACCACA 180
ATCTCCCAGG AGGGAGCTGG GTCCTGGGAG GAGGGCAGAG GGATCAGAGA GAGGGAGACC 240
AGGGGGAGGA GTTTCTGGCC CCAATTTTGT ACCAAAGCTG GAAAAAACAA AGTGTTGCTC 300
ATTCTTTGGA TTTTGGAAAA TTTGTGATAG ATTATAAGAC AGATTTTTTG GGGGGGTATT 360
GAAGAAAGGT GTAACCACTC ATTATCTGAA ACCACAGGCT GAATTTACTG CATGCTTAAG 420
CAAGGGACAG CTGTACTTGC AAGGCACAGC GTATCTCTGA GCAAAGCAGA GAATTAATCC 480
CATACAGGTT TTGGGAAGTG TGTGGTTTAA GGATGGGTCA ACGTGTGCTG GTTGATCTTT 540
GGCACAGTCA TTGGCATGCA GCTGTTGCCG ACTGGTTATT TTCAGAAGCG TGGGGCTAGT 600
CCTGATTGAG TGCATAGTTT CAGCAGCACA GTTACTGAAA CACATGGCCA TATAAACCAG 660
GTTTATAATT GGTTCTAAGA GTCACTTGAT ATCATAGCCA CATACCAATT AGTCTTTTCC 720
TAAGAGGGTG GGCATGTTTT ATTCTAGGGG GAAGAAGGGG AAGGGCAGAT AGCTCTATAT 780
ACACACAAAG AGGAAGGTCT CAGTAGAGCA GCCTGTGTGT CTTCTCCGCT GCTGGAGCTC 840
ATCTTGACTG GCCAGGGCTG GTTCCTAAGA AGGATCCCAG GCACCCAGAG CCTCCTGGGT 900
TTGGATGTGA GAGGAAAGTC CTGTGACCTC CTTTGCCTCT CCCATGTCTG GAGAGAAGCT 960
GTATTTCCGG CTAATCCAGG AGCGACAGCT CCAGGGTGCA CCCCAGGTTC TGACATGGGG 1020
ACTTGCAGCA CCCCCCCAGG TTGGACCCTG ACGTGCCTGG CACCCCTTGT GAACCCAAGA 1080
CCTCAACTTC AGCTTCTCCG CACAGCAGCC ATGGCCAGCT GTCAGCCGCC ACCTCCTCCG 1140
AGAGGCTGGA ATTCCTCGGG CAGATTTCTC ACCCTCGCAG GACTTCTTTC CAGCGTGTCT 1200
GGCAAGTGAG AGGGCTTCGC AGGCCCCAGG AGAGGCTTGT GGCAGAGAGG GCTTTGAAAG 1260
GGAGAGGAGG AGGGAGGGTA CTGCTGTTAC AGCCCAAGCC TTAGGCCCCC GCTGAGGACG 1320
TCAGGTGGCC CATGTCTGGA AACACCCAGC GCTGTGGCCC ACGTGGTGAC TCTTGGGTGG 1380
CCCAGGCTGG GTGTGTGGGG GCAGGGCCTC AGAGAAGAGA GAAGGAGAAG GGGAAGACCG 1440
AGGGCTGGGG GTGGCGGTGG AGAGGCCACT GAGGACAGGG AGTGGAACAA CCTTGCAGAG 1500
AGTGGTGCAG GGAGAAGTTA CTAGAATGGC AGCACCCTCT CCCGCCACCC AGGCGACACC 1560
TCTCGGGGAA CCCACCTCTG CGAGGGAGCC CTCAACTTCC TCCCGGCCTG ACCTGCCTGC 1620
TCGAGGGTTT CCACGGTCAC AAAGTTACCT CAGGGACTAG AAAAGAACCA TCTTTTTGGC 1680
CTGGAGCCTC TGAGGTGGGG CCTCCTCGGC CTCAGTCACA GCCAAGGTCA GGGGGAAGGA 1740
GAGCGCCCCA GGCTTCCCTC AGGAAAAGGA AGGGTCCGGC TTCTTTAGGG AAACAGCTGC 1800
TGGGATCTGG TGCTGACAGA CGGCCATCTT TCCACACCAA GGCTCTGGCC TGTCACCACC 1860
CTGTCTGGGG CCTCGAGTTC CCACCAGAGT TTTCATAGGG GCCTCTTCTG CTGACCCACC 1920
CAATCCACCC GCAGATGGTC TGGCCCGCCT CTCAGACTGG GAGCGGACCC AGCTCACTTC 1980
CCTACCGCCC CACTGCCCTT CTCTCTCTCC ATCCTCAAGA GGAGGTGAGG TGGTGAGGGG 2040
CAGTGAGCAC AGGCTTCGGA TTCAATTCCA CGTCAGTCAC TTATGGTACA GTTTTAAATT 2100
CTGACTCGCT TAACTTACAT GGCTTTGGAC CAGCCTGGGC CTCAGCTCCT TCATTTGTAA 2160
GATGAGGAGG TGGAAATGGA TTATTTGTAA ACTTTCTTTC 2200
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