| Tag | Content |
|---|
EnhancerAtlas ID | HS043-40723 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr8:8870550-8872030 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr8:8870980-8870998 | CTTTCCTTCCCAGCTTCC | - | 6.17 | | ZNF263 | MA0528.1 | chr8:8871801-8871822 | TTCTCCTTCTCTCCCTCCCTC | - | 7.83 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 8870850 | 8872023 | | chr8 | 8871177 | 8871841 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I009010 | chr8 | 8867821 | 8873230 |
|
Enhancer Sequence | GATAGAGTCT TGTACCCAGA CTTGAGTGCA GTGGTGCAAA CCCAGCTGAC TGCAACCTCC 60
ACCTCCTGGG TTCGAGCAGC TCTCCTGCCT CAGCCTCCTG AGTAGCTGGG AATACAGGTG 120
TGTGTCACCA CGCCCGGCTA ATTTTTTGTA TTTTAGTAGA GACAGGGTTT CATCATGTTG 180
CGCAGGCTGG TTTCAAACTC CTGAGCTCAG GCAATCCACC TGCCTCAGGT TCCCCAAGTG 240
CTAGGATTAC AGGCGTGAGC CACCATGCCC GGCCATTCTC ACTTAAAAAA AAAAAAAAAA 300
AAAATTAACA CTGCACTGCT GGCTTGAATA CTCTTTCCTT GGAGCATTTT CTTCAGGTAT 360
AACTTGTTCT GCTTGATTTT TCTCCAGCCC TACTGGATTC CCCACTTGCA GTTTTCTTTG 420
CTGGTTCCTC CTTTCCTTCC CAGCTTCCCC GTATCAGATG ACCCAGGTCT CAATCCTAGC 480
CCCCGTTCTC TGCTTACATC CTCTTCTCTG CTTACATCCT TTCGCTTGAT GATCTTATCT 540
AGTTCCATAG CTTTCAGAAG CTGTCTCTTT GCTGGTGACT TTCAAATACA TATTTCCAAC 600
CCGTTCCAAA TCCAGATTGC TTATTTGAAA TCTCTGCTTA AGTGTCTCAA CCTTTTGAAC 660
TTACCCCAGC CCATTCTATC TTTAGCCTCC TGTAGCCTGG GGGATGGCAG CTTTTTCTAA 720
TTAGAATCCT TCTAATTGCT CAGTTCAAAA ACTTTGGAGT CATCTTTGAC TCTTGTTTCT 780
CTCACATCCA GGTCATCAAT GATTCCTGTT TGGCTCTGCC TTCAAAATAT ATCCAGAACC 840
CAGTCACTTA ACTGAACTGC TGTGACTTCA TTCTGATCCT CTATCATTTA TGTGACTTAC 900
TGCATTCGCC ACCTAACTGG TCTTTGTGTT TCTGTCTGTG TCCGCCTACA ACCAGTTCTC 960
AAAAAACTGG CCAGAGTAAT CCTTTTAAAA TACAAGTCAT TTCACCCCTC TGCTCAAAAC 1020
CCTGCAATGG CTCCTCATTT AACTCAGAGT ACAACCAATA TTCCTTACAT GACCTGGCCT 1080
ATTGTTTCCT CTGATTGTTT CCTGTCTTAC TACTCTTTTC CTTAACTCAT TCCACTCCAG 1140
GCATACTGAC CTGCTTGCTC ATTCTCAAAA ATGCCAGGCA TGCTTTATCC CATTACTTGC 1200
CAGGACTTTA GCTCCAGTTT TCTTAGCCAG AAGTCTTGCT GGCTGATGTT TTTCTCCTTC 1260
TCTCCCTCCC TCCCGTTTTT CCTTCCAGTC CTTCCTTAAA TCTTACCTCT AAATAAAGCC 1320
TACTTGATTA TCCTATTTAA GAGTGTGGCC TGTGCCCATG TTTCTGACCC CCCTTACTGC 1380
TCTACTTTCC TTTGCTTGCT CAAGGGAGTC TCCTACTTTA TCTTCCTGAG TAGCTGGGAT 1440
TACAGGCACC CAGGTTCCTT TAGTTTTAAT AACCCTTACT 1480
|
