| Tag | Content |
|---|
EnhancerAtlas ID | HS095-18884 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr20:57638590-57640010 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr20:57638740-57638751 | AAACCACAAAC | - | 6.02 | | TP53 | MA0106.3 | chr20:57639518-57639536 | AACATGCCTAGACTTGAC | - | 6.15 | | TP53 | MA0106.3 | chr20:57639518-57639536 | AACATGCCTAGACTTGAC | + | 6.18 |
|
| | 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 |
| GH20I059063 | chr20 | 57638656 | 57639542 |
|
Enhancer Sequence | GGGATTAGAA ACAAGGGGAA TGTCGCAGAA GTCATTTGGC ACCAGGAGGG CTGTGCATGC 60
CCTTGTCTCT CTGCCTCATC CTTTGCTGCA CTTTCCTCCA ATACGTGAGT ACATATGTAT 120
ATATTTCTCT CACAGCCCCT CCTAATTCCC AAACCACAAA CACCGAAGCC TTATATAATT 180
TCACTGTGAT TTCTTTTCTG TTTTTGATTT ATCTGAAGTG TTGCTTGACT GCTTTATCTT 240
TCTCTACACA GCCTCTTAAA TTGCTTCAGC AGATCTAACC TCTCCAGAGA CCGGAGACAG 300
GCACAAAGCT TTACGCCGGA CACTGCCAGG CCCACGTCCG TGTGGGCGTT GAATGGATGC 360
TACGTGATGG CAGAATGAGT CACTGAGATT TAGGCGGAGA GTTTGGAGGA AGGTGCTAAT 420
GAAAAGGGCT CTGGTGCTGC AGGAGACATA CGCAGGTCAG GAATAATGAC GTCAGCCCGG 480
AGCCAGTGTT TAAAAATAGT GAAGCTCTTC TATGAATCAA AATGATTCTA TGGGGAAAAA 540
ACTAAACTGG TGATGGAAGG TTATATTGCT TTGTAAAAGA AAAAGTAATT TATGCTCGAC 600
TTCAAGAAAA GCAAAAGTTA CAAATCAAAA TAAACTCAGA AGTGCTTGAA GTAGGCAGAA 660
ACTCATCAAA ACAGTTGGAG TGAACTTACC ATGTTCTGTA CACTAACTAA AGAAAATTGC 720
TAGGGGATAG TGAATAGCAA AGATGCCTGG CTTCCTTCCC TATCGCAGTC ACCTCTGCAA 780
GTAGGATTAC CAGCTTCTGC TTTGTGACAG CTTTTGCTGT TTCTGATGGG TCCTTATGCT 840
GAGGGTACAG TCGACAGACC ATTCACTGCT GAAGCTGTCA GAATTAACCC CAAAGAAAAA 900
CGGAGCTGAA TAGGCTTTAT GATTACATAA CATGCCTAGA CTTGACCAGC CCAGGCTGTT 960
TGTTTATATA TGTCTGGCAT GCCAGATTCG ACCTGGCTTA AGTGGTACCT GCTTTAATTA 1020
ATTTAATTGG TTTTCTTTTC TTGATGGAAA ATAGAAAGAT ATTTAACTAC TCCAAAATCT 1080
CTTCCCTACC CCATGAAAGC CTTTGTAAAT TCTATTTGAT GAGGTGGTTA AGTTATTCAG 1140
TGAATGATTC TATGCAAGCA TATACTCACA AAAATAATAT TTAAACAATA CTATAGCTGA 1200
CATGGAATAA ATACCAAATA ACTAGTCAGA CCACATCTGT ACTTTTACAG TTGATCTTAG 1260
CCAAAGGCTA AGAAGCAATG CACCTCTGTA CTTCTAAATA CAAAATCAAT TCTGCAACAT 1320
AAAAACATTC ACCTATGGGA ATTGGGATTT TGGCTTTCTT TTAGTAATTC ATAAGCTTGT 1380
GGTAATAAGT ATAAAAACAG GAATTACCAA CTGAGTAAAA 1420
|
