| Tag | Content |
|---|
EnhancerAtlas ID | HS108-00632 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:20334650-20335900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr1:20335123-20335139 | TGTTGCCATGGCAATG | + | 6.14 | | RFX1 | MA0509.2 | chr1:20335123-20335139 | TGTTGCCATGGCAATG | - | 6.17 | | RFX2 | MA0600.2 | chr1:20335123-20335139 | TGTTGCCATGGCAATG | - | 6.66 | | RFX2 | MA0600.2 | chr1:20335123-20335139 | TGTTGCCATGGCAATG | + | 6.67 | | RFX5 | MA0510.2 | chr1:20335123-20335139 | TGTTGCCATGGCAATG | + | 6.92 | | RFX5 | MA0510.2 | chr1:20335123-20335139 | TGTTGCCATGGCAATG | - | 7 | | STAT1 | MA0137.3 | chr1:20335056-20335067 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr1:20335056-20335067 | TTTCTGGGAAA | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 20335000 | 20335304 | | chr1 | 20334929 | 20335259 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I020008 | chr1 | 20334567 | 20335901 |
|
Enhancer Sequence | CCCCTGAGAG ATGATGTGTG AGTTCTGATC CTCTGGAAGC AGATGCCAAG ATGTAGTTGG 60
AAATGTGAGA CATATATGGG GCAAAATAGC CATGAAAGCT AATGGGGGCA ATTGAGAAAG 120
GAGTAGGGAA AGAGAGTAAG TTGAAGCAGG GCAGGTGAAC CCCAAAATTG GGGCTTAGCC 180
TGGGAGGGTT CTTGGCTTCA CCCAGGAAGG AATTCAAGGC TGAGTTGGTG GTGTTAGCAA 240
CTTTTATTCA AACAACAGTA TGCAGCAGCA GTAGAGGTAC TGCTTCTTGA GGATCAGGGC 300
TACTCCATAG GCAGTGTGCC CAGAGTAGCA GCTCAGAGGC AGTTCTGTAG TCATAGTTAC 360
ACCCACTTTT AACCACATGT AAATTAAGGG ATGGATTATG CAGCAATTTC TGGGAAAATG 420
TTGATAACTT CTGGGTCATC ACGTTGCCAT GGAAAGGAGC GATAACTTCC AGGTGTTGCC 480
ATGGCAATGG TAAACTGACA CAGCACACTG GTGGATGTGT CTTATGGGAA GCTGTTTCTG 540
ATAAAGAATG GCTGGGTTCC CAGCTAAACC CCACCCTCAA GCTTGGAACC TTGGCCCTAA 600
GTGAAAATAG TGGACACAGC CCAGCCTGAA GGGTCAGCTG TTTTCACTTA GGGCCAAGGT 660
TCCAAGCTTG AGGGTGGGGT TTAGCTGGGA GCTCAGCAGT TCTGTATCAC TTCTACCCTG 720
ATACTGTTTT AGTTCTCAGT TTGGTCTGGT GTCCAAGCCC CATCTCTGGA GTGAAGTCCC 780
ACCTCCTACC TCAAAAGAAG AGAGAAAAGG AAGGAACATT GGGTAGGAAG AAGCTCAAAC 840
TGTGGCACAG CTCTGAGAAT GTCTCAGCAA TCTGATGAGG AGTTCTCAGG TGAACTATGC 900
CCATTAGAGG AGTCCTGCAC TGGGAAACAA TTACCTGGCT CTAGTCCCCT GTCATCACCA 960
TCATGGGAAG AGCACTGGAG AACATGGCTT TTTCATGAAT ACTGCGGCAT ATCCCAAAGG 1020
AACATGGGCT TGGGGCTGTC CACTAAGCAC ACTCCTTGAA CAGGTTCTAA TTTGAGGGGA 1080
GAGCTGATTG GTGCTGTCCA AGATTGTCAC AGGAAGGGTT ACTCTGGATT GGTTGGACTT 1140
AAGGACACTG AGCCTTTTTT TTTTTTTTCT GTTGGATGGG TCGTTGAGCA TTAAAAGCTT 1200
AAGGATAGAA GGTAGAGCAA CCAGAACTCT CACACCTTGC TGGTGGGAAT 1250
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