| Tag | Content |
|---|
EnhancerAtlas ID | HS095-15700 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr19:58998880-59000300 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:58998959-58998974 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | 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 |
| GH19I058488 | chr19 | 59000262 | 59001539 |
|
Enhancer Sequence | AAACTCCAAA TAAGTCCAGG CGCGGTGGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGGT 60
CGAGGCAGGG GGATCACTTG AGGTCAGGAG TTCAAGACCA GCCTGGCCAA CATGGTAAAA 120
CCCCGTCTCT ACTAAAAATA TAAAAATTAG CCAGCCGTGA TGGTGGGCGC CTGTAATCCC 180
AGCTACTCAG GAGGCTGAGA CAGGAGAATC TCATCAACCC AGGAGGTGGA GGTTGCAGTG 240
AGCCGAGATC ACGCCACTGT ACTCCAGCCT GGGCAACAGA GCAAGACTCT ATCTCAAAAA 300
ACAAATTAAC TACAAATAAA TATGAATAGG ACTAAAATAT GATAGAAACA TGGAGAAAGG 360
CCATAAGGCA GGAATACACA TCAGAAGAAA CTAGGCTGAT AGACCAGAAA GAAAATATGC 420
TTAGCATTAC ATGCCTAGCA GTAATCAGAG AAACCCCAGC ACTGTGAGGA CAGGGCTTCA 480
CCTGCCTTGC TCATGGCCAC ACACCCTGTT CATGGCACTG TGAGGGCAGG ACTTCACCTG 540
CCTTGCCCGT GACCACACAC CCTGTTCATG GCACTGTGAG GGCAGGACTT CACCTGCCTT 600
GCCCGTGACC ACACACCCTG TTCATGGCAC TGTGAGGGCA GGACTTCACC TGCCTTGCCC 660
GTGACCACAC ACCCTGTTCA TGGCACTGTG AGGACAGGTC TTCACCTGCC TTGCTCGTGG 720
CCACACACCC TGTTCATGGC ACTGTGAGGA CAGGGCTTCA CCTGCCTTGC TCGTGGCCAC 780
ACACCCTGTT CATGGCACTG TGAGGGCAGG GCTTCACCTG CCTTGCTCGT GGCCACACAC 840
CTTGTTCATG GCACTGTGAG GACAGGGCTT CACCTGCCTT GCTCGTGGCC ACACACCCTG 900
TTCATAGCAC TGGTTGGTAT TCGTAGCATT GTCAACAAAC CAGATACACA TCAATATAAC 960
GTGATGGATT TCTCAGCCTT CAAAATAGCA AGTTAAAAAC CCTGCCAATT AAAAGAAAAG 1020
GCATAAACAT GACTATGATA AAAAAAAAAA AAAAAAGGCT GGGTGCGGTG GCTCACACCT 1080
GTAATCCCAG CACTTTGGGA GGCCGAGGCA GGTGGATCAT GAGGTCAGGA GATTGAGACC 1140
ATCCTGGCTA ACATGGTGGA ACCCCGTCTC TACTAAAAAT ACAAAAAATT AGCCGAGCTT 1200
GGTAGCAGGC ACCTGTAGTC CCAGCTACTT GGGAGGCTGA GGCAGGAGAA TGGCGTGAAC 1260
CCAGGAGGTG GAGCTTGCGG TGAGCCAAGA TCACGCCACT GCACTCCAGC CTGGGTGACA 1320
GAGCAAGACT CCGTCAAAAA AAAAAAAAAA ACAAAAAAAT ACAAAGTGCC AATAGCAGGT 1380
ATTGGTGAGG AAATGAATAC CAGGACCTGT GCATATGATG 1420
|
