| Tag | Content |
|---|
EnhancerAtlas ID | HS138-18625 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr19:11734570-11736420 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr19:11736364-11736374 | TCTAATTAAA | + | 6.02 | | DUX4 | MA0468.1 | chr19:11734699-11734710 | TGATTGAATTA | - | 6.14 | | GATA2 | MA0036.3 | chr19:11736067-11736078 | TTCTTATCTTT | + | 6.62 | | MEF2C | MA0497.1 | chr19:11736247-11736262 | TGTTATTTTTGGCCC | - | 6.08 | | SPI1 | MA0080.4 | chr19:11736316-11736330 | TCCTTCCTCTTTTT | - | 6.06 | | SPIC | MA0687.1 | chr19:11736316-11736330 | TCCTTCCTCTTTTT | - | 6.38 |
|
| | 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 |
| GH19I011623 | chr19 | 11734483 | 11736248 |
|
Enhancer Sequence | CAGTGAGTGG AGATCGCACC ACTGCACTCC AGACTGAGCG ACAGAGCGAG CCTCCGTCTC 60
AAAAATAAAT AAATAAATAA ATAAACAGAG TAACCTTAGC TCTCTGAGTG CTAGTAAACT 120
CAGATCGAGT GATTGAATTA TGTGGTCTCT ACTAGCCTGC TGCTTTTCCA TGTTTACCAG 180
ACCCATCAGT AAACCGTGTT AAAGCCTTAG GTATGGGGGA GTGAAATACC GCTTCGAATT 240
GCCTTTTACT TAAACGAATC CTGATGATAT GAGGGTCATA ACTTAGCATT TGGACTGCAT 300
TAATCATTAA GATTGCTAGC TGAAATAGTA ATAAGTTTAA AAAGAAAATC TGAACGCGTC 360
TCTAGAAGCA GAGACTTAAA TGATATACTT TAACCATGTG CTTAAAACCA CGGGCGGAAT 420
AGCTTAAATC TTGTAATTGA GTTTTTGGGC TGACCAAGTT TATGGACTTT AATCTGGCAA 480
ACAGTCTTGA AAACAGTGAC TCACTGGCTG GGGAACTCAA TTTAGGACTC TTTTAGCAAG 540
TACAAATCAC ACTATCTGTA ATCAGTGGGT AAGACAGTCA TTCATGCATA AGTTTTCACT 600
ACACTTACAA CTTTTCTTCA CTTTCTGAGA AGGACACAAC ATTTTTACCT TCTAATTTGA 660
CAAATATCAT TTAATTAGGT TTAAAGTTCT CCTTTAAAGG GTAATGTGTG GTTTTACATG 720
CCTAGCTTTT AATTACTCAT TAATGAATTC GTGGGCCCTC TGTAATCTCT TTCCCTTCAG 780
AGGTTACTGT TTTACTTAAA TTGAATTTGG AAAGCTACCT TAGGGGTAGG AGAGAGATAA 840
CAGTGGCCAT TATTAGAAAA GAGGTTTTTC AAATTCTTAC ATTTTACTTA AATCTTAGCA 900
GAGAATCATA GTCTGGGACG TACGTAACAC ATGAACTTTT GCTATGGGCT GCTCACAGAG 960
CCAGAGGGCT GCGGTGCAGG TCCTTGGCGG CGGCCGCATT GTACTTGCTC AGGTTTTGCC 1020
TGTGTCTGCG CCGCTCCCTC CCTCCTTTGC CGGGGGTGGG GCATGCTGCC AGCCTGGGCG 1080
GACCTTGTGG GCTTGGTCGC TGCCAGCTTT TCTGCTGCTG AACCTTCTAT TCCGCCCACC 1140
GCTTGCTTGG TCGCGCGGTT TCGGCTTCTA ATGCCTTTTT TCTTTCTTTT TTTTTGAGAC 1200
GGAGTTTTTG CTCTTGTTGC CCAGGCTGGA GTGCAATGGC GCGATCTCGG CTCACCGCAA 1260
CCTCCGCCTT CCAAGTTCAA GCGATTCTCC TGCCTCAGCC TCCCGAGTAG CTGGGATTAC 1320
AGGCACTTGC CACCACGCCC GGCTAATTTT GTATTTTTAG TAGAGACAGG GTTTCTCCAT 1380
GTTGCTCAGG CTGGTTTCGA ACTCCCGACC TCAGGTGATC TGCCCACCTC AGGTGATCTG 1440
CCCGCCTCAG CCTCCCAAAG TGCTGGGATT ACAGGCATGA GCCACCTCGC CCGGCCTTTC 1500
TTATCTTTTT ACAGACATAC ACCTGCTTGC CTTGCCGATT TTGCATTACT GAGCAGGTTA 1560
AGAGCTCTCC TTCTAATGCT GCCTGCTCAA GACAGGGACT GATAGCTGTA GCGTATCCTC 1620
TGTCCTTTTT CCTATCTATT GGAGGAGGAG GCTTAGGTAA GACCTCTGTT TCCTCTTTGT 1680
TATTTTTGGC CCAGTGATAT TGGGGCTGAG GGAAGAGAAG GTGATAAGGC AGGTGACGTT 1740
TTCTCCTCCT TCCTCTTTTT AGGCTCTTCT GTGTGTAAAC TGAGCCAGGA CTGCTCTAAT 1800
TAAAGCCCAT AACGTTAAAG ATTTTACTGG GACCTGATGC CTTTGCACCT 1850
|
