| Tag | Content |
|---|
EnhancerAtlas ID | HS141-03284 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr11:46231410-46232550 |
Target genes | |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF8 | MA0652.1 | chr11:46231905-46231919 | GTGAAACTGAAAGT | + | 6.01 | | JUN(var.2) | MA0489.1 | chr11:46231809-46231823 | GTGAGTCATTCTCT | - | 6.15 | | KLF4 | MA0039.3 | chr11:46232047-46232058 | GGAGGGTGTGG | - | 6.32 | | ZNF263 | MA0528.1 | chr11:46232410-46232431 | ACCCACCTCTCTCCCTCCTCC | - | 6.36 | | ZNF263 | MA0528.1 | chr11:46232413-46232434 | CACCTCTCTCCCTCCTCCCCC | - | 6.73 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 46231590 | 46232206 | | chr11 | 46231600 | 46232200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I046209 | chr11 | 46231548 | 46232255 |
|
Enhancer Sequence | AGGTTGGGAA TGGTCTCTGT AAAGGATGAT GAATGAGAGG GGATGAGGAA TTAACTCAGG 60
GGAAAGCAGC ATTTGGAAGG CAGAAAGAAG AGTGAGTGAA GAAGAAAGAA TTGTTCAGTA 120
AGCAGGGGGT AACCCACAGA TACTGGTACC AAAATGCCAG GGGGATAAGG AGATTCAGGG 180
AGGGAGAAGA GTCAACAACG TGAAAATCTT TCACTGCTGC AGAAGTCAAG GAGGGCAAAG 240
ACCGAGAAAC ATCCCACAGA AAGTCCCTAG GAGAGGAAAC CAGGGAAAGG CTGAAAAGGA 300
GCAGAGGGAG GAAGCTAAAT CCAAGGGTTT ATTTTAGAGT GACCTTGCAG GCAAATGGGG 360
GGTGTTGGGA AGGTGCAAAA GAGGACACTG GCCTCAATGG TGAGTCATTC TCTTTCCGTT 420
TTTCTCTTGC CTTTCATGGT GCCAAGAGCT AGTCAGTGAC TCTATTCCTC ACCACTCACC 480
CGACTTGCAC AAGTGGTGAA ACTGAAAGTT GGGTAAGAGG ATGGAGGCTC AGCCTTGACC 540
CTAGGACTGG AGACCTGTTT CTTAGGCATG GTTCTGCTGT AATCACAAAT ACCTAATGGA 600
GGCTGGACCT CTGATCTCTT TACTTATAAG ATGGAGGGGA GGGTGTGGAA AGTGTTGCCT 660
GAAGCTAGCT GTGGTTTGGT GTTTGTCTAC ACCCACGGTG TCACATGGCT GCAGTAAAGT 720
GAGAAAAATA AGGCCGAGGT AATGTGTGTT TCATGAATGA AGTTAAATGT ATGCAATTTA 780
AAAGACCGTC CTTTATCCTG AGATTATGTT TTTCTTGGTT TGATTCTCCC TCTAGCATCT 840
GTTTTTTCTT TTTTTTTTCT TCCAACTTTT ATTTCAGGTT CAGAGGGTAC ATGTGCAGGT 900
TTGTTACATG GTAAACTGCA TGTTATGGAG GTTTGCTGCA CAAATGATTT TGTCACCTAG 960
GTAGTGAGCA TAGTACCCAA GAGGTAGTTC TTCTATCCTC ACCCACCTCT CTCCCTCCTC 1020
CCCCTAGTAG TCCCCACTGT CTATTGTCCC CCTCTTTGTG ACCATGTGTT CCTCAATATT 1080
TAGCTCTCAC TTGTAAGTGA GAACGTGTGA TATTTGGTTT TCTGTTCCTG CAGTAATTCA 1140
|
