| Tag | Content |
|---|
EnhancerAtlas ID | HS104-10658 | Organism | Homo sapiens | Tissue/cell | HUVEC | Coordinate | chr11:61962400-61964660 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr11:61964591-61964609 | ATATGGGTTTCCCTTTCC | - | 6.26 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAAGTACCCA GGGACACAAA AACTGCGGAA GGCCGCAGGG ACCTCTGCCT AGGAAAGCCA 60
GGTATTGTCC AAGGTTTCTC CCCATGTGAT AGTCTGAAAT ACGGCCTCGT GGGAAGGGAA 120
AGACCTGACC ATCCCCCAGC CCGACACCCG TAAAGGGTCT GTGCTGAGGA GGATTAGTAT 180
AAGAGGAAGG CATGCCTCTT ACAGTTGAGA CAAGAGGAAG GCATCTGTTT CCTGCCCGTC 240
CCTGGGCAAT GGAATGTCTC GGTATAAAAC CTGATTGTAC GTTCTATCTA CTGAGATAGG 300
GCAAAACTGC CTTAGGGCTG GAGGTGGGAC ATGCGGGCAG CAATACTGCT TTGTAAAGCA 360
TTGAGATGTT TATGTGTATG CATATCTAAA AGCACAGCAC TTAATCCTTT ACCTTGTCTA 420
TGATGCAAAG ACCTTTGTTC ACGTGTTTGT CTGCTGAACC TCTCCCCACT ATTGTCTTGT 480
GACCCTGACA CATCCCCCTC TCAGAGAAAC ACCCACGAAT GATCAATAAA TACTAAGGGA 540
ACTCAGAGGC TGGCGGGATC CTCCATATGC TGAACGCTGG TTCCCCGGGT CCCCTTATTT 600
CTTTCTCTAT ACTTTGTCTC TTTGTCTTTT TCTTTCCTAA GTGTCTCGTT CCACCTTACG 660
AGAAACACCC ACAGGTGTGG AGGGGCAACC CACCCCTTCA AAAAACAAAA CACCAACTGA 720
TTCTCTTGCA TGTCTGGGGG TCAGAAGCCC AACATTAGTA TCACGCTCAG GAGGTTGGAG 780
GCAGGAGGGC TCCACTTGCG CTGGGGGCTC TCAGGGAGAG TTCACTAAGG GCTGCTTCTG 840
GCTTCTGGGC TGCTGACCGT CCTGGTCCTG TGGCCACATT ACTCCAACCT CTGCCTCCAT 900
GATACATTCT CATCTCCTTT TTCTTCCAGG TTAACGCTCC CCGCTGCGAC TTATAATTAC 960
AAAATATAGG GTTTGAGTTT AGGCACCACC AGAATATTCA AAACAATCTT CCCATCTTAT 1020
GACCCTTACC TTCATCACAT CTGCAAAGTG CTGTTTTTGG ATCATGTAAC GGAACATTCA 1080
CAGATTCCAG GGATTAGGAA GTAGATATCT TTGGGGGAAT GGGGGCAAGA ATCAGCCAAC 1140
CACAGCTCCC CTCCCTCCTG CGCCCTAACA GTGCTCTACA TTCTATTCCC TCCATGGCCA 1200
CAGCATCACC TCTAAGAGTC GCTCCATTCC CATCAGACGT CACATCACAG CCCAGTCCAC 1260
ATCCTTCCCA GCTCAGACTA AGTCCCTAAA TTGTCTTGCA GCCTCCGAGA ACGCTTCCTG 1320
TAATACATCC TCCTCATTCA CGCCAAAGTG AGCCCCCTAA AACTGAAATG TGACACTATC 1380
ATCTGTTCAA CAACCCTGCA TGACCAGAAG GCACTTGTTC TCAAGGGTTT CAAGTAAGGG 1440
AACACAATAC TGAAAACACA CTTTCATAAA TAGTGGTTAT TTTTATACAG TGGAGAAAAT 1500
AGTAGATGAC AATTATTATT ATTATTATTA TTATTATTTG AGACAGAGTT TCGCTCTTGT 1560
CGCCCAGGCT GGAGTGCAAT GGCACGATCT CAGCTCACTG TAACCTCTGG TTCCCAGGTT 1620
CAAGCAATTC TCCTGCTTCA GCCTCCCAAG TAGTTGGGAT TACAGCCATG CACCACCACG 1680
CCCAGCTAAT TTTTTGGGTT TTTTTAGTAG AGACGGGGTT TCTCCATGTT GGTCAGGCTG 1740
GTCTCAAACT CCCGACCTTA GGTGATCCGC CCATCTCGGC CTCCCAAAGT GCTGGGATTA 1800
CAGGCATGAG CCACTGTGCC TGGTCGATAA CAGTTATTAT TAGGTAAGCA TTGATCTTAA 1860
GGGAAATTTG TATTTTTAAT CACATCAGGA AATATGTACA CTTAGAAGTA GAACCTAATG 1920
TGTGAAACTC ATGACCAGTT CAGCCTACTA CACACTATGT GTGCTGGAAA CAAGGATTCA 1980
TGGAGTTCTT CCAGCACTCA GAGACACCTA GAAGGAACCA CTGCCGGGGG AGCAAGTCCA 2040
CACCCTTATG TTGCACACAA GGACTTCCAA GGCCCTTTTC CTGCCAGCCC CTGTCCCTTC 2100
CTCTCCTTTC TCCCAGGTGC TCCATGCTCA GCCATTGCTG TTTATATTTC ATTTCTTAGG 2160
CCTCACATGA GTCACACCCT TGCACCAGGG TATATGGGTT TCCCTTTCCC TCTATAGCTT 2220
TTTGTTCCTA TGACATCTGA CAACCCCATC TTTAGAATCC 2260
|
| |
|
|
|
