| Tag | Content |
|---|
EnhancerAtlas ID | HS037-00748 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr1:38836000-38837470 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr1:38836761-38836774 | AGCTAATTAATTT | - | 6.15 | | Nkx3-2 | MA0122.3 | chr1:38836791-38836804 | AGAACCACTTAAC | + | 6.06 | | ZNF263 | MA0528.1 | chr1:38837183-38837204 | GGAGGAAGAGAGGGGAAGAGA | + | 6.65 |
|
| | 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 |
| GH01I038370 | chr1 | 38835996 | 38838106 |
|
Enhancer Sequence | AAATAATTGG CTCAGTCAGA CTGAAGGGAA GGATTTGTAA CTCACGTTAG TGGGAGACAC 60
TCACTCCCTC TTCTGCTAGA TGTCAACCAG GAAGATTGTA TTCCTTTCTT GCCAGGGGAG 120
GGGAGAGCCT ACTTTAGGAT AAAGCCAGTG TTGGGTATGG CAGAGTGAAG AGAGAAAGTA 180
GACCTATATC TTTGATGACA TTAACCCATC AATTAATTGT ACCACCCCTG CAGCCTGCAC 240
TAGCCCTAGT GTTCTCATAG GAAATAATAA ATTTTTGGAG AGCTTAAGCC AGTTTAAATA 300
GTATTTCATG TTTCTTGAAA TCAAAGGCAC CCCAATTGGA AAAGTCAGAG AGCAAGTCAT 360
CGATGGGCTC CGGATCTGAA GGCAGAAACT TGCAGATCCT GAGCCAATGC TCTTAACTGC 420
TCAGCGCTGG GCTCCCTCCC TTCCAGTTAG AGTTTGTGAC CTCTTTCTTA CAGATGAGAA 480
AGCTTAAGTT TAAATGGGAG AAGTGATTTG TCCAGGCTCA CAGAGTTAGC AAGTGGCTTA 540
CCCTGGCTCA GAATTCATGT TTATCCGACT GCAAAGCCCA CACTCTCTAC AAGCCTCTGG 600
TGGCTTCCCA CACTTGAGGC TGCCACCGTT CCTGTACCTT TGACTCCAAA CAGAGGCCTC 660
TCCGTCACCA AATAATGTGA TCAAATCAAA CCTTCTTTCC ATACAATTAG AAAACATAAC 720
AGGTTACAGC AAAAAATGCA AAAACCTCCA AAGCCGCTCA AAGCTAATTA ATTTCTATTA 780
CTAGTGAGAG AAGAACCACT TAACATGTCT TTTCTTATTC AAATTACCAT TGACGGCACC 840
TGCTTTTTTA TTCTTGGGAA ATCCTGCTAC AATGCGGGCA AATTATGTAA GACTGTAGAA 900
TTTATGAAGA TAAGGCAATT AGCATTACAA AACCGAGTCC GGGTTACAAT TTCTGGGGAA 960
CAGAAAGAGT TATGATGCTC CCTTAAATGG CCCAGTGAAG TCTCACAGAT TGAGTTACTC 1020
CTGTGGTAGT CAGGAAAATT GAAGGCGAAA CGGCGCCATG ATGGTGGGTA ATTAATTGTC 1080
TGGGCCCTTT GGTGATGGGG CTGTCTGTGC TGTGGAGGAG GCGGCCAGGG CTCTGCCTGT 1140
TCCCTTAAGA AGGAAAAGAA ACCGAACAGG GTTTCTGGGT TTGGGAGGAA GAGAGGGGAA 1200
GAGAAAGTTC CTCCTGAAGT CCCTGGTCCT TTGGGTCAAG GAGGGTTCTG CTCTGGGGTC 1260
TGCCCTCTCA GACGGTTTTC AAAAATCTCC ATCCTGCCCT GCAGCCCCAA CTCTCAGCAC 1320
AGCTGCCACT GAGCAGGTGC TTCCTTAGAG TGTTTAGATG TGCTGCTTAG ATTTTGCATC 1380
TGAGCTAGGA GGACTTTTTT TTTTTTTTTT TTTTTTTTTG TGACAGGGTC TTGCTCCATT 1440
GCCAAGGCTG GAGTGCAGTG GTATGATCAT 1470
|
