| Tag | Content |
|---|
EnhancerAtlas ID | HS098-03127 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:116657660-116659310 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr1:116658773-116658784 | AGGGTGTGGCC | - | 6.32 | | MEF2B | MA0660.1 | chr1:116658386-116658398 | GCTATTAATAGC | + | 6.14 | | MEF2B | MA0660.1 | chr1:116658386-116658398 | GCTATTAATAGC | - | 6.14 | | ZNF263 | MA0528.1 | chr1:116658440-116658461 | TAAGGAGGAGGAGGGGAAAGC | + | 6.36 |
|
| | 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 |
| GH01I116115 | chr1 | 116657699 | 116659217 |
|
Enhancer Sequence | AGGCTGCTAC CTGTGTTCTG TAACTTACTA ACTTTGGGAA CCTGGGCAAA TTACTTAAAT 60
ATTCTGAACT TTGGTTTCCT CATCTATAAA ATGGGGATAA TCATAGCATC CACCTTAAAG 120
AATGATGGGT AGGCAGGAAT GAGCCTACTC TTATAAAATG CCTTGCACAC AGGAAGGACT 180
AAATAATCTT AGTTTCACGG TAATGCTGCT GCTACAGCTT CTGCTACATT TGGGGGCTGC 240
AAATATTCTG CGTGACCCAA GCATTTGATT CATGGAAGAA TTAGTCTACA AAGGAAGGGA 300
TATGATGGTG GAAAGCCTAT GGTCTCGTGC GTATCTATCA CTGGATTTAA CTTTCCATTT 360
CTTTACATTA TTAGCCCCTG AAAGACAGAG ATGATGCCAG TTTTTGTTTT GTTGAAATTT 420
TTCTAACTGA TGATTGGATT TCATGCAATT CTGGAATTAA AGGTCTGACT TCTTGTTTTC 480
TGGAAGGAAG TCCTCAGCCT TTTCTTCTCA GTAACACTCA TTGGGAATGA CATACACATA 540
GTCTGCATGG TCATGGGTGT GATCAGGCCT GTGTGACATT CCTGGCATGC TACTTAGCAC 600
CACCACTCTG TCTCCATTGC AAGGAAGCGT ATCGGAATGC AAGTGAGTCA GAGTGATATT 660
ATTATAGGGG ATAACCTTAA ATCCCCATAA TTTATATTTG AAGCAGTAAA TTATTCATGA 720
ACTTGAGCTA TTAATAGCAG CAAATGACTT GTGGGGCAAC AATGAACCTG ATGCTGTGGT 780
TAAGGAGGAG GAGGGGAAAG CAGCCCAAGA TGGGACAAGG ACCTTGACAG CATGGAGACA 840
TGCCTGGGAA GAGCAAGGCC CAAACAACAT TTGTTTCCAT GTTTTGCCAT GAACTAAGTT 900
TGGTGACAAG GTTGCCTCAA GGCTGCCTTG AAGCTGCAAC TGGTATCTTG CTGGCTTCCT 960
AAAGTTTGAG AGGCAGTAAA GGATTTCCAG GGTTGGGCTT GCAATGGGTG TCTACTTGTG 1020
TTAGAGCCTC CTTCTTTAGA TCACTGTACA GCTGCCCCAA CCCCACTGCC TGCTTTTCCA 1080
CACCCTGAAA TGAACTTCTT GCTGTATCTG TCTAGGGTGT GGCCAGAATA AGTGGAGAGA 1140
AACAGTCTGG GGGTTCTGTG TTGTCACACC ATGAGGGTGA CAAGAGGTGT CTGGCACTAA 1200
GCCTGGAAAC CCCCAGCACA AATCACTTCT GGGGCTACCA AATAGCACGG TGATGCTGTG 1260
TGGGTAAGAA CTTATTGCAG GAAGTGTAGC CAGAGATGTG GGGAGGGACA AGGCTGCCCG 1320
CCACCTAGAG AAAGAGGCTT CTGCTCAGGT CCCACAGCAG GAGCATCACT GTCTGGCCCT 1380
TGCTGCATGA CCCTTTGTGC TTGTTAGATG CCAGAACAGT TGCTGATGCC TAAATACATG 1440
GAGACCTAGG ACTCCTTATT TCATGAGTCT TGACTTTAAA TTGAAGGCAT TTTTAGGTTC 1500
AGGAAGAGGA TAAAGGGTAG GCCGTACTTC TGGTACATCA GTACTTAAGG GTGTGGCAAA 1560
GTGTGATGGA AAGAAGTGTT GGAGAGCCTG TCTAATTCTA CATCTAACTG CCGGTGTGAT 1620
GTTAGGAAAG CTGCCTTGTC ACTCTGGTCC 1650
|
