| Tag | Content |
|---|
EnhancerAtlas ID | HS080-30864 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr6:41906190-41908100 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr6:41906263-41906275 | CAGTAAACAGAA | + | 6.02 | | GFI1 | MA0038.2 | chr6:41907002-41907014 | CCAATCACAGCA | + | 6.02 | | STAT1 | MA0137.3 | chr6:41908050-41908061 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr6:41908047-41908061 | CCTTTTCCTGGAAA | - | 6.91 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_25452 | chr6:41898485-41910935 | DND41 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 41906927 | 41907077 | | chr6 | 41906447 | 41906530 | | chr6 | 41907242 | 41907431 |
|
Enhancer Sequence | GGAGCCAGAA GTGAGACAGA TAAATTACAA CGCTACCCCT AGTGCATGTC CCAGGAGCCA 60
ACTCCTAACT CAGCAGTAAA CAGAAGGGAC TCAGCTTCTA AGGAAGCATC TGGAAGGCAA 120
CTGGGAGTGG GACTCTCCCT ATGGGGAGGC AAGGGGTTGT GTTTGAGGGA AAGTGGCCAC 180
CTTTCCCCAT ATCCAGGCAA CCAGAGAATC CCAGTGTTAA CTGGTGGAGA ACACACCCCT 240
GGGAGTGCTT AGCTTCAGTA GGTGGCAGCG GCCATCACAT TCCTGACTTT TAAGGCAACC 300
TGGTCTAGCT AGAAGACCCA GGTTCTACAC TCATCTGCTC AGTGCGATGC TGAGGCAGGA 360
CCTTGCCCTC CTTCCTTGGG CCTCAGCCTC CTCTGCTGCA CACGGATTTG GACCAACTGG 420
AGTTCTCAGA GGTCCCTTCC AACCTTGACC TTCTAGGAAG TCTTTTGGGC ACTCCACCCC 480
CAGCTCAGGC AGAGGGAAGA GTACTTTTTG CCTGTACTGA AAAACCCTCA TACGTGGGCA 540
CACAAACCAC CTCCATCTTT TCACAAAAAG GAAGTTCCCC TTCTACCTTC CAGCCCCAAC 600
CCCTCCAAAA ACATCTTGCT CTCTGGCCCT GGAAACTAGC TCCACCTTCA GACTTGCCAA 660
AAACTACCAG ATTCATCACA AAGAGCTGTG GCGCCTCCTG GATTCCCAAC TCTGGCCTCC 720
TACTCCCATC TCTGAGCTAC TTGGCAGGAA GAGGAATCCT GTTCCTCGAC TCACAGCAGT 780
CGGGGGCCCC AGTACCCTGG CTTCCCTGCC AGCCAATCAC AGCAGCCTGC TTGCTGCCCT 840
CCTCCCTGGG AGATGGGGCC CAGAGACTCC TCTCAGGGTC AGCAGAAGAC TTGGCCCGCC 900
ACAGAGCAAG GTGGAGGAAG GTGCCAGCTC ACCCACCCTC TCCCCCAGCC TCCCTAGGAG 960
ACAATCTGCA TGTCCTAAAT AACCTCTTCC AGATCCAGCA GCTCCCCCGC CTCCTCCCCA 1020
GGCTCCTTCT GAGGCGGGAC AGAACCGGTG ACTTTCCTGC CCGGCCTGAG CCCAGCCCAA 1080
GTTTCCAGCA AGAGGCCCAG GGAGCCACTT CCCAAACCAC AGGAGTGACA GCAGCTCCCC 1140
ACAGGGTTAT GAAAGACCTT GGTCAGAGAG GGCGGGCCAG GGGAGGGGGC ACCATTATCA 1200
CATCGGAAGC AGATGCAGCT CACCTCCCTG TCTGTCCCTC AGCTTGGGCC TTGGGCTAAG 1260
GGGGGAAGAG GGAGCTGTTT CCACCAGGCC CAAAGCAGCT GCTCCAGTTC CTCAGAATGA 1320
GGACGAGGAA GGATTAGGAA GAAGCTGTTT CTTCCGGGAT ATAAGAGGAA GCAAAGAAGG 1380
TGGGATGAAA TACATCAGCC CTTCCTTAAA GCAATCAGGG CCTGGCTTTA ATTGGCTCTG 1440
GGAGGCTTTT CTATCACAAA GTCCACATGA GGATAAAGAC TCAACCAAGG CAAAACCCCC 1500
TCCCCCACAT GAAGCACATT CCACTCCCCT ACTCCAGTGG GGGTGTGCAG GCATGCCCTT 1560
CTGCTGCCAA TAAATAACTC ATGGTGGCTG CGTAAACCCA GAGGCAAAGT ACTAGTGAGT 1620
GTAGACATGC AATTTGACTT GTTGCTATCT GGGGGAAAGA CCAGGAAGGA GTGGCATCCC 1680
CTGGAGGTCA GGAGGAGGGG GTTTAATGCC TGCCTGCAGC TCAAGCCTGG GCGGGAGTGA 1740
TACTAACCAT CACACCACAA TGCCCCATCG TTTGTTCCAC CCCAATTCCT TTCCCAAAGG 1800
TCCTGATCCC CTTGCTTCCT CTCCAGGGGG CAGAAAGCCT CTGATATCTC AAGCTTTCCT 1860
TTTCCTGGAA AGTGGGGAGA CAATACGTGT CGGGGGTGGG GGGAGTTACA 1910
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