| Tag | Content |
|---|
EnhancerAtlas ID | HS095-00426 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:20497250-20498760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAX | MA0058.3 | chr1:20497856-20497866 | ACCACGTGCT | + | 6.02 | | Zfx | MA0146.2 | chr1:20498499-20498513 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH01I020171 | chr1 | 20497696 | 20498750 |
|
Enhancer Sequence | GCAAGGCTCT GGACTCAGGA GCCCTGGTCA AGGCTTCAGG AGCAACTGGC TGCTTCTGCT 60
CTGAAGGGGC AACGTGGGAA GAAAGTACAG CCCAGGCCAC GTACTTTCGG GTCCAACTCC 120
CAGCCCTGGC TGGCACCTCC CACCACTGCC CAGCAGTGCC ACTGCCTGGG GCTCCAGCCT 180
CTGCTCCTCA ACCTTTGCTC CACTCTCCCT CATCTCCTGG GGTCCTGGGC TGGGAGGGTG 240
AAGAGCATTG AATAGAGAAG CTTCCCTGGG TGCAGAGAGC CTAGGCCAGC CCTGGCGAGT 300
GCAGCCAGCC CACAGGAGCC CAGGGTGGAG GCTTGGGCTG GGCCAGCCAG GTGTCCCCAC 360
CCCTGTGGCA AAGACAGGTG GGAAGAGGCC ATGGGAAACT CGATCCCTGG AGGCCACCTT 420
CTCCAGTCCC CTCTCCCCAT CCCTCCCACC AGGCCCTGAT CCCTTCCCCT CTCCTGAACA 480
TGGCCTTGGA GGTGTCACAG AAAAGACACT TTGCTTTAGG CCTGAGAAGG ACCACACCAG 540
AGAGCTCCAA CTCAGGAAGT CTCCTTGAGC TCACGTGGGG AACAAAAGGG GGTTCTTTCC 600
CTGTCAACCA CGTGCTGGTG GCAGTGGGCA GGGCAGGCCA AGAGCTGAGG CAGGTCCTCC 660
CGGTGCAGGG GTCCGAGCCC CCAACCCACA CAGCTGGTGC CAGGGAGACC TCACAGTCCT 720
AACTCTGGGT ATTGGTGTGT GCTGAGCTGA AGTGGTGGGT TGGGGGAGCT CAGGAGACCA 780
GGGTTCTGAG CCCTGGAACC CACTACGGGA TGGAGGATGT ATCTCCCGCC ATAGGGGATG 840
AGTGGCAGAG AGGTGGTAGT TCCCTGACCT CAGGAGGAAA CAGAGGAACT CCAAGGTGCA 900
CTCACAGCTC TGAATAAATA CACCTGGGAA GGAAAGTGAT TCATGCAACC CCACGAGGCC 960
AGGCAGGAAG TGAGCCACAC ACTATAAGAA GCCACTTCTT CTTTTTTTTT TTTTTTTTTT 1020
TTGAGACGGA GTCTCGCTCT GTGGCCCAGG CGGGAGTGCA GTGGCGCAAT CTCGGCTCAC 1080
TGCAAGCTCC GCCTCCCGGG TTCACGCCAT TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG 1140
ACTACAGGCG CCCACCATCA CGCCCGGCTA ATTTTTTTTG TATTTTTAGT AGAGACGGGG 1200
TTTCACCGTG TTAGCCAGGA TGGTCTCGAT CTCCTGACCT CGTGATCCGC CCGCCTCGGC 1260
CTCCCAAAGT GCTGGGATTA CAAGCGTGAG CCACCGCGCC CGGCCAAGAA GCCACTTCTT 1320
TATTTGTTGC TCTTCACCCT CCCAGCCCAG GACCCCAGGA TCCACCCTGG CTATGCTGGA 1380
AAGGATGGTG CTCACGAAAG ACTACTGTCC CGTGCCTCCA AATGTGCCTG CTGTCTAGGC 1440
CAGGATTGCC CTGCACATAC CCATACCCTA CCAGCCGCAG AACACGCTCC GGATGCCAGG 1500
GCCACGCCCC 1510
|
