| Tag | Content |
|---|
EnhancerAtlas ID | HS104-59721 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr8:145987000-145988170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr8:145987373-145987383 | GACACGTGCC | + | 6.02 | | Klf1 | MA0493.1 | chr8:145987739-145987750 | TGGGTGTGGCC | - | 6.62 | | NFIC | MA0161.2 | chr8:145987075-145987086 | TCTGCCAAGAA | - | 6.02 | | Npas2 | MA0626.1 | chr8:145987373-145987383 | GACACGTGCC | - | 6.02 | | RAX | MA0718.1 | chr8:145987128-145987138 | GCCAATTAAC | + | 6.02 | | ZNF263 | MA0528.1 | chr8:145987022-145987043 | CTTCTCTCTTCCTCCTGCTTC | - | 6.59 | | ZNF263 | MA0528.1 | chr8:145987016-145987037 | CCCTCTCTTCTCTCTTCCTCC | - | 6.89 |
|
| | 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 |
| GH08I144760 | chr8 | 145986139 | 145989574 |
|
Enhancer Sequence | GTGTGGCACC TCTACCCCCT CTCTTCTCTC TTCCTCCTGC TTCCACCGTG TAAAGTGCTG 60
GCTCCCCCTT TGCCTTCTGC CAAGAAGCAG GTTCTGCCAT GCTTCCTGTA CAGCCTGCAG 120
AACCATGGGC CAATTAACCC TCTTTCTTTA TAAACTACCC AGTCTTGGAT ATTTCTTTAT 180
AGCAGTGTGA GAATGGACTA ATGCAATATG CTAAAGAAGG GGTGGGTTGG CCAGGTGCGG 240
TGGCTCACAC CTGTTATCCC AGCACTTTGG GAGGCCGAGG CAGGAGGATC ACGAGGTCAG 300
GAGATCAAGA CCATCCTGGC CAACATGGCA AAACCTGTCT CTACTAAAAA TACAGAAATT 360
AGCCGGGCAT AGTGACACGT GCCTGTAATC CCAGCTACTC AGGAGGCTGA GGCAGGAGAA 420
TCACTTGAAC CTGGGAGGCG CAGGTGAACT GAGATTGTGC CACTGCACTC CAGCTTGGGC 480
GACAGAGTGA GACTCTGTTT CAAAAACAAA AAAGAAGGAG TGGGTTATTC ACAAGTTTTC 540
TACAAAAGGA GTGGGCAGTT CCCTGAACGG AGGAACCCTC TCTTTTAAGC CGTATAAGGG 600
GAACCTGTGG TGCTGCTATG GCATCTGTAA ACAGTCACAC GCTGGCGGGC ATGTCTTATG 660
CTAATGTATT AATTACAATT TGCGTGTAAT GAGCAGTGAG GGCAACTAGG GCTGTTCCTA 720
TCCCCATCTT TGTCCTGGCT GGGTGTGGCC AGCTGCCGCA CTGCATCCTG CCTGGATCAG 780
CCAGGCCTCC ATTGTTGCTG GGAAAAGAAG TCCCATGGGG GGCCCACTTC ACATCCTGCA 840
CTGAGACGCA CACAAACCCT GGTGCGGCCT CCAGCCCTCA GGCTGACCCG GAGTGACCAC 900
TTCACATCCC GCACTGAGAC GCACACAAAC CCTGGTACGG CCTCCAGCCC TCAGGCTGGC 960
CCGGAGTGAC CACTTCACAT CCCGCACTGA GACGCACACA AACCCTGGGG CGGCCTCCAG 1020
CCCTCAGGCT GGCCTGGAGT GACCACAGCC ACTTTAGAAT GTGTGCCAGA GGCAGCTTAA 1080
TGTCACCAAA AGAACTTGTT CCAAGCAAGC CCGGGAGGAC AGGGGAAGAG AAGAGACCTG 1140
GTCAGTGGAG GAGCCACAGG TAACAGCTGG 1170
|
