| Tag | Content |
|---|
EnhancerAtlas ID | HS099-00329 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr1:19037850-19039320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:19038211-19038222 | CTGAGTCATCC | - | 6.32 | | IRF1 | MA0050.2 | chr1:19038249-19038270 | CCCCTGTTTCTCTTTCTCTTC | + | 6.28 | | JUNB | MA0490.1 | chr1:19038211-19038222 | CTGAGTCATCC | - | 6.14 | | RREB1 | MA0073.1 | chr1:19038221-19038241 | CCCCCACCCTCCAACACACA | + | 6.09 | | ZNF263 | MA0528.1 | chr1:19038973-19038994 | GGGGGCAGGGGAGAAGGAGGA | + | 6.12 |
|
| | 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 |
| GH01I018711 | chr1 | 19037661 | 19039354 |
|
Enhancer Sequence | CCCTCGTCAC ACCCCCCTCA CCTGTGCCCT GGCCTCCACC TCTGCCTCAC TGCCATCCCT 60
TCTGTTTCCT TCCCTCTGTT CCCTTCTTTT ACTTCCCTGC TCTCCTTGAC CCCCTTCAGT 120
TAACTGGACA ATGCTTGAGT TGGTTTCCTA TCCAGGGCAA TGTAAGGGGT TCTGCTGACC 180
TAAGTCTGGG GAGGAGAAGG TGCCAGGTGC AGGGGGTTCC CTCTCTGCAG AAAGCAGGGG 240
AAAGGCTGTC TCCTGCTCCT CCCTCAAGCC CCTGGGGAAG GACGAGCTGA TGGAGGAGTG 300
CTTGACTCAA GTTGGCAGGG CATGGGCTGA GTGGTTTTTC CCAGGATTAG GGGAAAGCTA 360
ACTGAGTCAT CCCCCCACCC TCCAACACAC ATCCCCACAC CCCTGTTTCT CTTTCTCTTC 420
ATGACCAGTG CGGTTGGTAC AGAGTCAGGG GTCAGTTTGT GGAGTGGACC AGGAGTCCGT 480
GGCTGGATCT TCTTGGACCT GAAGCCGAAT GACATTTTTC AGTGTCTGCC CTCCCCAACT 540
GGCCTTCTGC ACCCAGGAAG AGCCCAGCTC CCAGAGACTG CTCCCCTGCC CCACCCAAAC 600
CACATCCACC AGCCCCTGGT CACAGCATCA GGCTAACAGT TAGGCTGCCC GTCCACTCTG 660
CTCATCAGGC AGCCCCCAAT CCCCCAGGGC TTTTTCCCCC GGTTCTCTTG GCGAGGCCAG 720
CCCCAGGGTA GGGATGAACT GCAAGGCTCA GGGAAGCAGC CAAGGCGTAG GTGTGAACTG 780
ATGGTCAGTG TGAATTGATG GTCAGTGTGA ACTGACGGTC GCTTTAGTCC TTGGCCCTGA 840
GCATCCTCAG CCCTTCCAGA ACCTGGGGAG ACAGACCCGG CCAAGACCCT GCTCTCACAT 900
CCAGCTCCAT CTTTGTCCAC AGTTAACCCA CCTCAGTGGG AAACGCTCAG TTATTTCCCC 960
CCGGCAGCTC CTCACCAAAC AAAACCACCT GCTCAAGTCC ATCAGAGGCC TCAGCTCCAG 1020
CCCACAAGGG AGCGGCCTGG GCAGAGCCTC TTCTCCTGTG AAAATAGACT CGTGTTTATG 1080
TCTCTGCCTT TCCTACCCCT TTTTCCTGGG TGGAGGGAAA TGAGGGGGCA GGGGAGAAGG 1140
AGGAAACCCC TCCCGGAAAG AAAGGCTAAA CCAGGATTAG GAACTTTCCA GACTGCTGCT 1200
GAGGGGAGTG GAGCATGCCT ATGAGTAGGC TCTGCTAGGA ACTGGGAGGC CTGGCGGATT 1260
GCCTGGCTTT CAGGGTGACA TTAGAGCCCT TGGATCATTG AAGGAGAAGT GGGAGAGCAA 1320
CCCTGACCTT GCCTCCTTTC TTAGAGAACT GGGTAGAATT CTGGGAAGAT ATCGGGTCTT 1380
CAGCCCACCT ATCTGAGTCC GAACAAGAGG TGGGTGGAGG GTGGCCTTCA AGGACCACTC 1440
TGGGGCCGGG TGTGGTGGCT CACGCCTGTA 1470
|
