| Tag | Content |
|---|
EnhancerAtlas ID | HS073-12605 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr6:106204880-106206220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr6:106205984-106205996 | AAGTAAACAGAT | + | 6.74 | | FOXP2 | MA0593.1 | chr6:106205984-106205995 | AAGTAAACAGA | + | 6.32 | | NFAT5 | MA0606.1 | chr6:106205221-106205231 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr6:106205221-106205231 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr6:106205221-106205231 | AATGGAAAAT | - | 6.02 |
|
| | 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 |
| GH06I105757 | chr6 | 106205011 | 106206345 |
|
Enhancer Sequence | GTGTGATGGT GCATGCCCAT AGTCCCAGCT ACTCCAGAGG CTGAGATGGG AGGATTGCTT 60
GAGCCTGGGA GGCGGAGGCT ACAGTAAGCT GAGATCACAC CATTGCAATA CAGCCTGGAC 120
AACAGAGTTA GACCCTGTCT CAAAAAAAAA AAAAAGTTCC CAAGGACATA TCATCCTAAC 180
TCAGTGTGCA TTTACATGGA TAAGGCTGAG AGGAAGGAAG TTTGGAGAGA AGACAGATTG 240
GAAAAGAGAA GGCACTAGAA ATGAGTTAGG AGGGAAGGTC CAGATGGGAA ATGAACGTGC 300
CAGAATTAAG GTTGTAGGGA GGAAAAGAAG AGGTTACGCT TAATGGAAAA TCCAGGGTTC 360
AGGGAACCTA GTGACCAGTT GGATGTGGAG ACAAGTAATT CCTTTGGGAA AGATTTTGTG 420
AATTTAGTTG GTCTGTTCTC CTCTTTGAAA TATTTTTATA ACACTCCTTT CCAAGGGGGT 480
GACTTTACCA GAATGACAGC TTGCACTTTC ACCAATGTCC ATTCACTGGT TCCTAACCCT 540
GAAATCTAGC CAACTAAGGT ATTAGGACTT CAAAAAAAAA TCAACATGGT GGTGTGGTTT 600
TCACCTTGAA ATGGGGTATT TACTCCTCCT CTAACAATAG ACATGTTGTT TCTGTCTTCT 660
AGGAGTTTCA CTTTGATGTG TCAAAGGAAA TGCCATGAAC TCTAGGGGAG AGTCATCACT 720
GCGTGAATGC AGGATAAACA GCAGGTGTGG CTGGGGCTTT AGGACAAGTG CCAGTCGTCC 780
TATTCCATTT TTAGAGATAA AAAAAAAATG AATGTTTCAA GTGCTTTGGT TTTCAGGAGT 840
CAAAGACAGC TTTCAAAAGA GTCCACGAAT AGAAGCCCAA CATTTCAGAG TGAAGCTGCA 900
TGACAGAGAC ACTTCTTAGT GTCTCCATGA TCATGATTAG GAAGCCGAAA CCAACACACT 960
CTTCTTTGCA TCACTTGGGT GAAGCAGGTG GGAGGCAGAT GTCCTGCCTG CACACCTGGG 1020
TAGGTTGAAG GCAGCTCTTT AATTTGAACA TTGAGCAATC ACCTTCCCTT TTAGAACCTT 1080
GCAAATTAAA TTTGCCCTAG GAACAAGTAA ACAGATGATC TGGCAAAAGC CAGGTCCAGG 1140
GACCGGAAAG AGATCATAAT ATTAATAATA ACCCCTTACA TTTGCATTGT TTCTGTATCC 1200
TTCACACAGC GGTCCCAGTG AAATGATCAT GTGCTTATTC TTGTCTTCAC TGGAAAGCTA 1260
AGGAGTCTAG GGCTTAGAGA ACTGTCTTGC CCCAGGTAAT AGCAAAATAG AGGCAGAGCG 1320
GAGACAGGTT TTCTGACGAT 1340
|
