| Tag | Content |
|---|
EnhancerAtlas ID | HS104-61841 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr9:126982690-126984180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr9:126983886-126983901 | ACTGGCCTTGAATTT | - | 6.42 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09686 | chr9:126975691-126986742 | CD14 | | SE_59974 | chr9:126945864-126986288 | Ly4 |
|
| | 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 |
| GH09I124220 | chr9 | 126982280 | 126986678 |
|
Enhancer Sequence | CCTAGCAATC GCTTATGCAA CACGCTAGTT CTCATGACAG TTCTATGAAG CAAGTACTGT 60
GATCACTATG ACTCCTATTT AACAGAAGAG AAAACTGAGG CATGGAGAGA TCAAGTCACG 120
CAACTAGTAA ATGGCAGAGC TGATCTGAAC CAAACTGTTG GGCTCCTAAG TCCCACCCTT 180
AACCATTACA CTATGCCCCC TTCCCATTTC ACCATCAACA GCTCTCTCCC CAGTCAGCCT 240
CACTCAAGCT CAACGCCGCT CTCCTTCTCA GAATTTTACC CAGGGCCTCC AACTCAGATC 300
AATAACCAGC ATCTGCTCCC AAGGGTAACA CCTGACACCT GACTTCTCAC CTTTTTCCCA 360
GGCCTGGGGC CCTGGAGTCA CCAGGGTTTG AGTCCTGACT TTGCCCATTT TCCAGCCGTG 420
GAGCTTGTAG AAGGCACTTC TCTTCCTAAA GCTTCCGTTT CCTCCACTGC AGCATGGGGA 480
GGGAGGCTTG TCCTAAATTT GTTGGCCTGT GGTGGAGACA ATTTGAAGCC ACACTCACGG 540
AGCAGGTCAC ACTGGAAGCG TATGTGTGTT CAGTGTGTTC CCTGGAAGCG TATGTGTGTT 600
CAGTCCATGA AACTCTGATC AACAGTTAAT CATATCCCCA GAGTCCTGGG GACACTGCCA 660
AGTATTTCTT TGCTTTTCCC AACACGTTCT CAGCCCCTGC AGTGTGCATC GTGGGCAAGT 720
GTGCTGGGCA GTCCTGTGTG CTTGCCCCTC TCCTGCAAAC TGCTTTTCCC AGTTTCCTTT 780
GCCAACTGGC TTCCTGTTAG GTTGGGCCAA GGGGAAGCAC TGGCAGGAGA TTGGAGCATG 840
GGAGGAGGGG ACAATCTGGG TATTTCTCCC TCCCTCTGCT TAGGGAGGGA GTGGGAGTGG 900
CCTTTCCCCA GCACAGGCTG CTCTCTTCTG TGTCTTTGGC TGCTCTAGAA CCACCCGGTC 960
ATCTGCAGTT CCAAGTCTCC AGGTGGCTCT GATGATTCAA GTTACTCCTG GGCAGTATCA 1020
CTGCCTCTTC CTTTTGTCTC TCCACCCCTA AGTGGTAGCA CCTTTTGCCA TTGTGGAACA 1080
AGCACTTGCC TCACCATTTG CTGTTTGGCT TTTCAGCTCT TCCCTCTTCC AGGTAACCAA 1140
TTCCCTATAT TAAATTTCCT CTGTTGGAAA TACCTAGAGT GGTTTCTGTT TTTCTGACTG 1200
GCCTTGAATT TTACAGCGGG CATCTTTGGC CCAAGAATTG TCTCTCTCTT CTCCACTTAC 1260
AGAGTTTTTA TCCTAGAGGG GCAGCATCAG ACCCCTGAGG GCATGTCACA GGCGGGACTA 1320
ATGGAAGAGG CTCTAGCTCC TTCTAGCTCT TTGCAGTAAA CTTACTACAA GACAGCAAAG 1380
CTTTCTCATG CTACCACTGA CTGTCTCTTG TGACATAGGT GGAGTAGCAT TGCGCTACTC 1440
TGCTGTCTCT CTACTTCACC TTCCTGAAGA CTTATTGCAC AAAGGGTGGG 1490
|
