| Tag | Content |
|---|
EnhancerAtlas ID | HS113-39227 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chrX:73096050-73098360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chrX:73098233-73098244 | TATGTAAACAT | + | 6.32 | | KLF4 | MA0039.3 | chrX:73097003-73097014 | CCACACCCTCT | + | 6.02 | | NR2C2 | MA0504.1 | chrX:73096632-73096647 | AGAGGTCAGAGGTTA | + | 6.91 | | Nr2f6 | MA0677.1 | chrX:73096633-73096647 | GAGGTCAGAGGTTA | + | 6.04 |
|
| | 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 |
| GH0XI073877 | chrX | 73097300 | 73098060 |
|
Enhancer Sequence | ATTTCACCCT CACATGAGTC TATCCTGAAG GTCTCTTAGT ATTAATAATT GGAGATTCAA 60
AGCAAGAAGC TGGTGAGCCC AGCCATTGCC TTCAGGCAAG CTACTCCCTT TCATGATCAT 120
TTTTTTCCAG GAGGCCTCCA CTGAGAAGTC TGCATCAACC CTGCCCTTCT GCAGAGTTCC 180
CAGTGATTTT AGGCTAAGGG CTTCTACTCT ACCCCTGGGG AATGTGACCC TTGCGTATCT 240
TCTCAGCAAT AACCCCATGG GCTCTGGGAC TGTACCCCTC TTCAACCTTC CCTGCTTCTG 300
AGATTTCAAT CTACAAGCCA GCTCATCAGG ATGCAGACTC CTATCCCTAA AGTTGGGTAA 360
CTGGCAGGTG ATGGCTGAGG GACCCCCATT CTGTTGGGGC CAACACACTG GGATGGGCAG 420
AGTGAGAGTA GGGGTCCTTT GATTCTCTGC CCATGTTCCC TTGGTCAGAC AACAGAGACA 480
AATCCTGCAT CCTTTGCTTT GCCTGTCAGT ATTCAGAGTT GTGAGTGAGG AAGGTTAGAG 540
ATCTGGAAGA CTCTGTATAG CCCTGCTGCA GAGGGAACAG CAAGAGGTCA GAGGTTACAA 600
TAAGAACAGT AACTCAAACC AGTTTCTGCC CCTACTGTCC TCCATGTTCC TGTGGAAACC 660
AAACTGCTGC TATGACCATA CTGCTGTTCT CTCTATTGTG ATCTATCCTC TCAACAACAG 720
AAAAAAGACA TAAAATATTG TTTCCAAAAG AAAGACACAA CCTGCAGCCA CAATGCAAAG 780
GAGCAGGCAG AATACACACA GTGTGAACCC ATGCTTCCAT GGCTCCATGC AAGCTAAGGC 840
TTGCCTGTTT CAGTAACAGG CCCCACATGT ACCTGCCCCA CCCTTGCCTG AATGCTGTGG 900
CTTTGGGTGA ACTCCCAGAG GCTGCCAACT CCCAGAGGCC GCTGATAGGC CCTCCACACC 960
CTCTGCCACT GCTGCTTCTG CCCCTGCTGC CCACAGGCCA GGGCAGCAGG CACCTTCATA 1020
GGCCCCAACA GTGAAATCCA GAACTGCTTC TGTGGAGGAA AGTGCAAGCA GGCCGCATGC 1080
TCCACAGCTG CCAGTCTTTA CTGCCTCAGA AGAGGGGGCC TGCCCTCCCC AGTGAAAGTC 1140
TGACAGCACA GCTACCCTGC TCTTGCCAGA CCATTTCAAC TGCAGCCCAG CCCCCATAAG 1200
CCTGTTGTCT CCCTGCCCCT GCCTAAGAGT TCTGCCAGTG ACCCAGGGAC CAGACTACCA 1260
TTCTCAATCA CATCAAGCAC CTGAAATGTG GGCTGACACA GTCCTGGTCC AGCCCCTTTC 1320
AGACTCATAC ATGACATTCA ATGGGCCATA TAGGGGCCTG AGAATAGAGG AGTCATCTAC 1380
TCTAGTCCAC CACTGCTGGC ACCTGACCAC CCCCACCCCC AGGGTCGGAG GTTGGACCAG 1440
CCCAACCAGC CAATATCACC ACAACTGACA CCCACATACA CAGGCCAAAT GACAGAGCCC 1500
CTACTCCTTT CTACATGAAG CAGCAGGGTT GCTCCATCAG AGAACAGGCA AGCCATAAAT 1560
CTGTCTGTAT TGAGCTGAGT GAAGAGGTTC CATCCCCAAA CCACTCCAGT GGAGAACTGT 1620
GAGTCAGGTA ATTTCCATGG CTCTCAGCTA CACTGTGGCC TGGAGATAGA AAACAGTGCA 1680
TCTGAAAGGA GAGTCATTAG CACCAGGACA GGGGTGTAAA GGAGAAACAG ATCACATTCC 1740
TGCATATCTA GGGTGTGAAG TCAGTGCAGC TCCCTTACCC CCTGCAGAGA CCTTGGTGCA 1800
TCTCACTAGG AGCTCCCCCA GCCACCCCAG TCAGGGCTGG TGCCTTCACT TGTCATTGGG 1860
ATATTTATGG GCAAGGCAGG GCTGGTGCCT TTGCTTGTCA TTGGGGTATT TATGGGCAAG 1920
TCAGGAGTGA TTACATACAC AGCAGCTTGT GCCCCAGCTG GGTCTTTGTT AGTGCCACTT 1980
ACTGGCCTGC AGGTCTGACT GCACAGCCCA ATGTAAAACC TAATAACAAA AGTGCACAAC 2040
CAAAGGCAAA GAATTTACCC AACATACACT ACAGTTACAC TCTCTAGAGG AAATATATAT 2100
ATGTGTGTGT ATATATATAT GTGTATACAC ATATATGTGT ATACGTGTAT ACATATATAT 2160
GTGTATACAT GTATACATAC ATATATGTAA ACATACATAT ATACGTATGT ATATATACAC 2220
ATATATACAC GTATATACGT ATATATGTGT ATATACGTAT ATATGTGTAT ATATACGTAT 2280
ATACACGTAT ATATGTGTAT ATACACGTAT 2310
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