| Tag | Content |
|---|
EnhancerAtlas ID | HS043-40790 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr8:11843390-11844950 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF13 | MA0657.1 | chr8:11843949-11843967 | CAGGGAGGGGCGTGGCCT | - | 6.51 | | KLF14 | MA0740.1 | chr8:11843952-11843966 | GGAGGGGCGTGGCC | - | 6.25 | | SP1 | MA0079.4 | chr8:11843953-11843968 | GAGGGGCGTGGCCTG | - | 6.62 | | SP3 | MA0746.2 | chr8:11843953-11843966 | GAGGGGCGTGGCC | - | 6.18 | | SP4 | MA0685.1 | chr8:11843951-11843968 | GGGAGGGGCGTGGCCTG | - | 6.64 |
|
| | 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 |
| GH08I011986 | chr8 | 11843710 | 11844709 |
|
Enhancer Sequence | ACGCAATAAC TGAACAGGAA AACCATAGGA ATCTATTGAT GTTTTGAAGG AAGCAGGAGA 60
CTGCAGCCTA CACTGAGTCA GTCGAAGGGC TGCGAGTCCC CTGAGTGTGA CAGAGTGAAT 120
TTGCCTCTGG GATACACATC CCCACTAGGG ATCCTGAAAG TCCAGGACAC AAGGTGGGGG 180
TGCTGGCGGG GAAGCCCTAA CCCGAACTAA CGCAGGAACC GACTTGGGGA TGGTTATGGA 240
CTATAAACTA TTCCATACTT TTAGGGGGAG ACCCTTGCAT GCACTTCCAG ATCCCAGCGT 300
AGATTAAGTG CAGCCATTCC TTACTGTTCC TCACAGGAGG CCTTGCGGCC AGCTACAAAG 360
TTCAGGCGCT GGTTGCAGTT TGAAAGAATC TCCCAACGGG GTTCACAGTA CAACCTCGGT 420
GGGGACGAAC TTCCTTGGCC AGGGCCGGGG CGGGGAGGGT GAAAAGCGGG CTGCAAGTGC 480
AGGAGCCGTA GGTGCAGAAG TCGTGGGTGC AGAAACTGCA AGTGCAGGAG CCACGGGAAC 540
ACGCCGGCTT TGCAGCGGAC AGGGAGGGGC GTGGCCTGAA CGCCTGGACT GCAATCTCTG 600
CGGGGAAAGC TTATGACTCC CGGCAGCCGC GAGTTCTGAT TACAGGCTGA CAGGAACTCA 660
GCTCGCTGCT TCCAGTGGAA CACCGTGGGA GTGGATCTGC CTTGTCAAGT GGGTAGGAAC 720
TGTGGAGCTT ACCACCGCCT GCTACTCCCT ACTTCTTGCA CAGACTCTTC TGTGCAGCAG 780
GGGCAGCAAC GCTGCCCTCT GAAACATTAA CCTAGTGGCC TGAGACCCGC TCCCATCCCC 840
CAATACCCAT AGAAGCTCCT TCTTTCTCTG CACACGGAGA CCAGTGTGCA GGCCCTCCCG 900
ACCCAGCCCC TACCTGGCTT TGCCCGGCCA CCCGCCCTGG TAACTCAACG CAAAGGACAG 960
AGTCTCCTGG GAGCGACATG GCCCCGCCCA TGTCCGGAGA AACCAGAGTA TCCCCCTCTG 1020
GGCAACATCA GGCAAGCAAA AATCCCAGGG CTACTACCGC AGCTGCTGCT CTTTTGCAAG 1080
CGCCACCTCC TAGCTGGAGG CCAACCCACA CAGTCCTTGA CAGTATCTCC TGGTAGATTA 1140
ACATTGCACC CAGGAAGGAG AAAACCGCTA TGGGATCTCA GCTATCACTG CTGCCTGCAC 1200
CACTCTGGCT GAACAGGAGG TCCTGAGTCC GTCCACATGA CCAGTTCATT ACTACTATAA 1260
CCCGCATTCA AGAAAGCTAA CATACTAAGG CTATCAATAA CAAAGGAATT TCACAGAATC 1320
TGTGTCACAA CCTTGCCACT CCCATTAGAG CTGGTGCTGC TACCCACTGC AGGGAAACTT 1380
GAGCATAGGT CACATAACTG GATCCCTTGC AGACATTCCC CAACACCAGC CTCGAGTGTG 1440
TCAACTTCTC TGGGCAGCTA GACCCAGAGG AGCAAGAACA CTCACAGTGA CCTGGCTCCC 1500
AGGGACTTCC AGGGACTCCC ACTTGCAGGG GAAGGAGGAC TGCATCACAT CAAGGGAACA 1560
|
