| Tag | Content |
|---|
EnhancerAtlas ID | HS138-00234 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:15294460-15296620 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr1:15296255-15296272 | TGGATTCCTAAAAAGAA | - | 6.19 | | RARA(var.2) | MA0730.1 | chr1:15295068-15295085 | AGGACACGTGAGGGTCA | + | 6.03 | | RREB1 | MA0073.1 | chr1:15294491-15294511 | GGTTGGGGGATGGTTTTGGG | - | 6.25 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26798 | chr1:15294684-15296104 | Esophagus | | SE_53292 | chr1:15293321-15296336 | Spleen |
|
| | 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 |
| GH01I014967 | chr1 | 15294172 | 15298701 |
|
Enhancer Sequence | AAGACAGTTT TTCCACGGAC CAGGTGTCCG GGGTTGGGGG ATGGTTTTGG GATGATTCCA 60
GGGCATTACA TGCACTACAT TTCTTGTGCA CTAAATTTCT ATTATTATTA CATTGTAATA 120
TATAGTGAAA TAATTATACA ATTCACCCTA ATGTAGAATC AGTGGGAGAC CTGAGCTTGT 180
TTTCCTGCAA CTAGATGGTC CCATCTAGGG GTGACGGGAG ACAGTGACAG ATCATCAGGC 240
ATTAGATTCT AATAAGGAGC ACGCAACCTG GATCCCTCAC ATGCGCAGTT CACAAGAGGG 300
TTCGTGCTCC TATGAGAGTC TAATGCCATC GCTGCTGATC AGACAGGAGG TGGAGCTCCG 360
GCGGTAATGT GAGTGATGGG GAGCAGCTGT AAATACAGAT GAAACTTCGC TCGCTCGCCC 420
CTCACCTCCT GCTGTGCAGC CTGCTTCCTA AGAGGCCAGG GACCAGTACC AGTCCATGGC 480
CTGGGGCTTG GGGACCCCGT GTGAAGCCAC TGCATTGTGT CACTTTGTTA CAACAAGAAT 540
GGGAAACGAA CCAGGCCCTC TCTTTCCCTG GACTTGGCAG CCCTAAACAC TGCCCTCTCT 600
CAGGGCTTAG GACACGTGAG GGTCATCTGT TTCCTTTAGA AACGCCTGCA GGGCACAGCA 660
GCCAGCACGG GGCGGGTGGA GTTAGCTAGC ACTGACTGAG CATGGAGCAG AAGAAAGGAT 720
CCGGAGTTTC CTCTCCTTAC TGGAAGGACT AAGGCCTGTG GGAGCCTTTT CCCTGCCACA 780
GAGTGAGTCA CCTGCCTTAC ACTGAAAGAA ACACAACTTT ATTATTTAAT TTGCTCATTC 840
ACCAAATGTT CCCTGAAAGC TTCCCTACCC CAAAGCTTGT GCCGATGCCT GTGGTTCAGA 900
GCATTCCAGG CCCTGCTCAG AGTCTAGGGA CATGCCTGAA ACCTACGACA CACTCAGTGT 960
ACCTTACTTG AATCCTATTT TTCCAAGTGG CCAACCAGGC CTGTAGATGA GAGTCTATCC 1020
CATAGGCATT CCTGCTTCAA GGAGTTCTAG GCTGCAGAGA CTGTCTTAAG TCCAGCGGGG 1080
TCGGTGGGGC TGGAAGACTA AAGCTCCCAG CAGGTGCAGC CATGCCCTGG CTGCCTTTGC 1140
AGATGTCACC AGGCCTGCAG ACAGTGGGGT AGTAGGTGGC CTGAGAGGCT GTTGAATAGA 1200
ACGATGTGTC ATCTGTGCTG GGGCGGCCAT GCCCACTTGC TTTCTTAGAC ACACATCCTT 1260
GTCACCACAG CACTGTGTGG GTTTGAAAAG CTACTTGATG TTTCCTGTGT CCCTTCCCAC 1320
ATCCGCACTC CATTCTTAGT CTCATTCCCT CCATCAAAGA CGTGTTCATC TTCTATGCAG 1380
TTCATCACCT GGGGTTGAAT GTGTATGTTC CTCTTTAGTA AATTCATACG CTTGAAGCTA 1440
CTGCTGTTTC TTTAGCCTGG TGGCTCTCGG GGCTGCTGCA GGGGGCCCAC CCTGAGCCAG 1500
CCCCTCGGTC CCACAGCCCT GACGTAGAAG ACTCTTTGCT GGTAAATCTC GGAACTCACT 1560
GGAAGCTTCC ACAAAGTTTA ACTCTACAGA CAGAATGTCT TCCTTACATA CTACCGGCTG 1620
CTTTTAAATA TTGTTAACAG ATCCCCCTTA AAGGCTTCTT AGACTCCACA TTTTGATCCA 1680
GTTGATAATA ATTGATGGTC AGGTGGAAGA ATTGCCCAGG CTCTGTTGTT GTTCTGTTAT 1740
AGTTGCCACT GGACCTGCTT TCAGCACCCT CACCCTGGCT GCTTCAGAGG GCAGCTGGAT 1800
TCCTAAAAAG AACCCATGCC CTAATGCACA AGTACTTTTT ATTTTATTTT ATATTATTTT 1860
TCGTGGGGGG ACAGAGTCTT ACTCTGTCGC CCAGGCTGGA GTGCAGTGGC ATGATCTTGG 1920
CTCACTGCAA CCTCTACCTC CTGGGTTCAA GCGATTCTCC TGCCTCAGCC TCCTGAGTAG 1980
CTGGGATTAC AGGCGCCCGC CACCACGCCC AGCTGATTTT TGCATTTTTA GTAGAGCTGG 2040
GGTTTCACCG TGTTGGCCAG GCTGGTCTTG AACTCCTGAC TTCAAGTGAT TCACCTGCCT 2100
CGGCCTCCCA AAGTGCTGGG ATTATAGGCA TGAGCCATGG TGCCTGGCCC ACAAGCACTT 2160
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