| Tag | Content |
|---|
EnhancerAtlas ID | HS138-35477 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr6:41905960-41908100 |
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 | GGGTTCCCAG ACCTGGCCCC ATTTCTGAGT TGCACACATG AGGATTTCTT CATTGTTTTA 60
TCTCAGGAAG GAACTTGTGG GTTTGACTCC TTATTGAGGC AGAAATGGCA ACCCCACCCA 120
ACCTCTTCCA GGCCCCAGCC ACAGCTGTCT CTCTCTTGGC CCCAGCTTAG GTGTCAGCCT 180
CTCAAATCAA CCCCTACCCT CACAGAGCCC CAGAGAAAAT AGCCTGGCCT GGAGCCAGAA 240
GTGAGACAGA TAAATTACAA CGCTACCCCT AGTGCATGTC CCAGGAGCCA ACTCCTAACT 300
CAGCAGTAAA CAGAAGGGAC TCAGCTTCTA AGGAAGCATC TGGAAGGCAA CTGGGAGTGG 360
GACTCTCCCT ATGGGGAGGC AAGGGGTTGT GTTTGAGGGA AAGTGGCCAC CTTTCCCCAT 420
ATCCAGGCAA CCAGAGAATC CCAGTGTTAA CTGGTGGAGA ACACACCCCT GGGAGTGCTT 480
AGCTTCAGTA GGTGGCAGCG GCCATCACAT TCCTGACTTT TAAGGCAACC TGGTCTAGCT 540
AGAAGACCCA GGTTCTACAC TCATCTGCTC AGTGCGATGC TGAGGCAGGA CCTTGCCCTC 600
CTTCCTTGGG CCTCAGCCTC CTCTGCTGCA CACGGATTTG GACCAACTGG AGTTCTCAGA 660
GGTCCCTTCC AACCTTGACC TTCTAGGAAG TCTTTTGGGC ACTCCACCCC CAGCTCAGGC 720
AGAGGGAAGA GTACTTTTTG CCTGTACTGA AAAACCCTCA TACGTGGGCA CACAAACCAC 780
CTCCATCTTT TCACAAAAAG GAAGTTCCCC TTCTACCTTC CAGCCCCAAC CCCTCCAAAA 840
ACATCTTGCT CTCTGGCCCT GGAAACTAGC TCCACCTTCA GACTTGCCAA AAACTACCAG 900
ATTCATCACA AAGAGCTGTG GCGCCTCCTG GATTCCCAAC TCTGGCCTCC TACTCCCATC 960
TCTGAGCTAC TTGGCAGGAA GAGGAATCCT GTTCCTCGAC TCACAGCAGT CGGGGGCCCC 1020
AGTACCCTGG CTTCCCTGCC AGCCAATCAC AGCAGCCTGC TTGCTGCCCT CCTCCCTGGG 1080
AGATGGGGCC CAGAGACTCC TCTCAGGGTC AGCAGAAGAC TTGGCCCGCC ACAGAGCAAG 1140
GTGGAGGAAG GTGCCAGCTC ACCCACCCTC TCCCCCAGCC TCCCTAGGAG ACAATCTGCA 1200
TGTCCTAAAT AACCTCTTCC AGATCCAGCA GCTCCCCCGC CTCCTCCCCA GGCTCCTTCT 1260
GAGGCGGGAC AGAACCGGTG ACTTTCCTGC CCGGCCTGAG CCCAGCCCAA GTTTCCAGCA 1320
AGAGGCCCAG GGAGCCACTT CCCAAACCAC AGGAGTGACA GCAGCTCCCC ACAGGGTTAT 1380
GAAAGACCTT GGTCAGAGAG GGCGGGCCAG GGGAGGGGGC ACCATTATCA CATCGGAAGC 1440
AGATGCAGCT CACCTCCCTG TCTGTCCCTC AGCTTGGGCC TTGGGCTAAG GGGGGAAGAG 1500
GGAGCTGTTT CCACCAGGCC CAAAGCAGCT GCTCCAGTTC CTCAGAATGA GGACGAGGAA 1560
GGATTAGGAA GAAGCTGTTT CTTCCGGGAT ATAAGAGGAA GCAAAGAAGG TGGGATGAAA 1620
TACATCAGCC CTTCCTTAAA GCAATCAGGG CCTGGCTTTA ATTGGCTCTG GGAGGCTTTT 1680
CTATCACAAA GTCCACATGA GGATAAAGAC TCAACCAAGG CAAAACCCCC TCCCCCACAT 1740
GAAGCACATT CCACTCCCCT ACTCCAGTGG GGGTGTGCAG GCATGCCCTT CTGCTGCCAA 1800
TAAATAACTC ATGGTGGCTG CGTAAACCCA GAGGCAAAGT ACTAGTGAGT GTAGACATGC 1860
AATTTGACTT GTTGCTATCT GGGGGAAAGA CCAGGAAGGA GTGGCATCCC CTGGAGGTCA 1920
GGAGGAGGGG GTTTAATGCC TGCCTGCAGC TCAAGCCTGG GCGGGAGTGA TACTAACCAT 1980
CACACCACAA TGCCCCATCG TTTGTTCCAC CCCAATTCCT TTCCCAAAGG TCCTGATCCC 2040
CTTGCTTCCT CTCCAGGGGG CAGAAAGCCT CTGATATCTC AAGCTTTCCT TTTCCTGGAA 2100
AGTGGGGAGA CAATACGTGT CGGGGGTGGG GGGAGTTACA 2140
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