| Tag | Content |
|---|
EnhancerAtlas ID | HS089-02116 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr10:104299840-104301250 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr10:104300135-104300146 | AGTGACTCATG | + | 6.14 | | KLF4 | MA0039.3 | chr10:104301012-104301023 | CCACACCCTGC | + | 6.62 | | Nr2f6(var.2) | MA0728.1 | chr10:104300191-104300206 | GAGGTCAGTAGTTCA | + | 6.07 | | RARA | MA0729.1 | chr10:104300191-104300209 | GAGGTCAGTAGTTCAAGA | + | 6.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTTCTGGCAC AGTAGGAAAT TTCAGAATCA TTTTGTACTT TGCCAGCCCA GGAATCAGCC 60
ATTTATCCAG GAAGCCCTGG TTTTATTTAG TGGAGAATGG TATATAGAAG CCATGATCCG 120
GAGGCTAGGT ATTATCATTG CTCTTGGAGT GTCACTGCTC CCAGTGGCCA GAACTAGGAA 180
ACACACATGC ACATATACAC ATACCACTCT ATTTCCATAT TGGTTTCTCT CTTAAATACC 240
ATGAATTCAT ACTGATACCT CCAATTCTAA AGCTATACCT ATGGGGGCCT GGTGCAGTGA 300
CTCATGCCTG TAATCCCAGC ACTTTGGGAG GCCCAAGTGG GTGGATCACT TGAGGTCAGT 360
AGTTCAAGAC CAGCCTGGCC AACATGGTGA AACCCCGTCT CTACCAAAAA TACAAAAATT 420
AGCCAGGTGT GTTGGTGCAC ACCTGTAGTC CCAGCTGCTC AGGAGGCTGA GGCAGGAGAA 480
TCACTTGAAC CTGGGAGGCA GAAGTTGCAG TGAGCCAAGA TCACACCACT GCACTCCAGC 540
CTGGGCAACA GAGCAAGACT CTGTCTCAAA AAATAATAAC TAACTAACTA AATAAATACT 600
ATACCCGTGG CATTCATTCC TGCCTGCCTT TAAAATATAT ATATATATAT ATTTCAGACC 660
AGGCACAGTG GCTCACACCT ACAATCCTAG CGCTCTGGGA GGCCAAGGTG GGTGGATCAC 720
TTGAGGTCAG GAGCTCGAGA CCAGCCTGGC CAACATGGTG AAACCCTGTC TCTACTAAAA 780
ATACAAAAAT TAGCTGGCCG TGATGGTGTG CGCCTGTAAT CCCAGCTACT CGGGAGGCTG 840
AGGCAGGTGA ATCACTTGAA CCCGGGAGGC GGAGGTTGCA GTGATCAGAG ATCGCGCCAT 900
TGCACTCCAG ACTGGGTGAC AGAGCAAGAC TCCATCTCGA AAAAAAAAAG TTACTTGGGT 960
TATATCTTTT CTTCCCCCTT TCAGTGTGGT TATATGGTTG ATTTGAAATA CTGTTAGGTT 1020
CATTAATTTC TGTTTGTATT ATATTTTAGC ATTTTCTCCC TCCTCATTGA TTCTGTTTCA 1080
TTTATTTTGA GTATGTGAAA GCATTATCAC GGATCCAAAA CCAAAAGTGA GAACTATACA 1140
AAAAGGTATA TTCAAATAAA TGTTACCCAC CTCCACACCC TGCAGTGCTT TCTACCGCCT 1200
TCCCACCTAC TGTATGTAAG AATCCATCTC ATTCATTTTT GGTTTATCCT TCCCACATGG 1260
CTTTCTACAG AAATGAGTAG GTAATGTATA TTTTCCTACT TTTCTTTCTT TCTTTCTTTC 1320
TTTCTTTTTT TTTGAGATGG AGTCTCGCTC TGTCACCCAG GCTGGAGTGC AGTGGTGCGA 1380
TCTCGGCTCA CTGCAACCTC TGCCTTCTGG 1410
|
