| Tag | Content |
|---|
EnhancerAtlas ID | HS043-41070 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr8:27153770-27154920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr8:27154523-27154533 | GGGGATTAGC | - | 6.02 | | Mecom | MA0029.1 | chr8:27154456-27154470 | CATTATCTTATCTA | - | 6.32 |
|
| | 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 |
| GH08I027295 | chr8 | 27153509 | 27155099 |
|
Enhancer Sequence | CTGTCAACCC ATCACCTAGG CATTAAGCCC CGCATGCATT AGCTATTTAT CCTGATGCTC 60
TCCCTCTCCC CAGTAATTCT TATCACACAA AAACATCAAG AACACAGCAT GGCAGGAAAA 120
ACCAGCAAGT GCAAGGTCAA CTCCTGCCCA CTCACCGTGG GCAATGACGG CCTCACTGTA 180
AAGGAACAAA CACCAGAACT TTCACTTTCC TCATCGACCT GATAACTGAA TTTAATAGAA 240
AAAGTACTAA TCAGGCTGGA ATTCTAGGGG CTTCCCATGT GACCTCATTA CCCTTAGCCT 300
CAGCAAAAAG CTCAGGACTC CTACACTCCC TGGGATGGGC AGGCAGTGCC ACCACACAGA 360
CAGACAGATA CTCCCTAAGT ATCCCCAACC CAGTCCTGTA CAAGGCAAGC CAGTCATATG 420
GCTTTAGCCA CAGAAGGAAA CCAAGTAAGA GAACAATGAT AAAGCTACAT GACTCCACGA 480
TGACTACTGG AAAAACAACT CAACAAACTC CAGCAACAGC AGGTTCGTAA TCGCTATTTG 540
GAGTTGGAAT TTCAACATGT ATTTATGGCT CTGACATCGG ATGACAAAAT AATCTACTGA 600
ACAAAGTGAA AACTCTCTCC CACCAGTTTG TTGGTCTATT AGACATCAGA AATGTTAAGG 660
ACTTGTCTCT GTTGGGCACT TGTATGCATT ATCTTATCTA AATTTTTTTT TAAAAACCCT 720
AGTAAAAGGG AATTGCCCTC TTTTTACAGA GGAGGGGATT AGCTTGGAGG GGGTTGAGGG 780
ATTTGCTGGG GAACTGGGCT TAGATTTGGA AATAGGTCTG CTTTGCGGTT ACTGCCCTGG 840
CACCCAGTGT GTCACATAAT CCTTTCTTCC ACACTGTTCC ACCAGCTCTG TGGCTCAGGG 900
TAAACTCCAC AGCCAAATGT TAATGAGGCT CTTTCCTGGG ACTAATCCTC ACCTATGGAC 960
ACATGGTGGA GGGGACCGCA GGCTCCTGAG GACAGCGCCC AGCAACCTGG ACCAGGCATG 1020
GCTCAGCTGT GGCTAAGATG AGTCTAACAG AGTGGTAATT ACTAGAAGCA ACCACTTCAG 1080
AAAGCCAAAG ACCAGAGCCA AGATCAACAG TCAGAAACAA GGTTGCCAAT CCACACAGGA 1140
CCTGGAGGAA 1150
|
