| Tag | Content |
|---|
EnhancerAtlas ID | HS007-02587 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr10:133775020-133776870 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr10:133775941-133775962 | TTCCGTTTTCATTTTCCTTTT | + | 6.3 | | Nr2f6(var.2) | MA0728.1 | chr10:133776450-133776465 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_47883 | chr10:133774821-133775236 | Pancreas | | SE_47883 | chr10:133776060-133776372 | Pancreas |
|
| | 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 |
| GH10I131961 | chr10 | 133774987 | 133776470 |
|
Enhancer Sequence | TGGGCACTGG GGTGATACTG GGCTTGGCTT TGAGCTCCGT GCCTCTGTGC CCCATACGCC 60
CCTCAGATCT CTGGTGACAG TGCGGGGCTG CCTACAGGAC ACCCAGGGCT CCTTGATCTT 120
TTAGGAACTG CGGCACCCCC GAAGCTGTGA CAGGTGCAGA GGCGCTGCCG TCCTGGGCCG 180
GGCCTCACCT TCCGCCTTGT GTGCTCTGGC GCCAGCACCC AGTCCCAAGG GCACAGCGGC 240
TGCGACTTGC CTCTGGCCAG GGCAGGTGGT GGTGTCATAC CCAGGACGGG AACCCACACT 300
TGATGTCCTC CAGGGTTTTT TTTTTTTACA TTATCTTAAG GACTGACAGT CTCCCACCCC 360
ATCTGCTCCC ATCTGTCCCT AATTTCATGC GCCTCCGCCT GAGTTCCTGC ACGCATTTCC 420
TGAATAAACA CACCCCTGTG CCAGTCAGAA CCCGCGGGGG TTTTGGAAGT GAGAGCCCAG 480
CAAGGCAGCT GGCCAGGGGG CGGCACTGCC CTCCGGGGAG CACCGGTGCC CGGGACTCTG 540
CTTCTGAGGC TGGCCTGTAC GATGATTTTG TATAAATATC TCCAATCAGA ACCTTTTTAG 600
TGTATTTCTT AATATAACAG AAACTGGTGT CTTAAAATAC AAGACTAGCT GCCCGGTGAT 660
GACACCAAAT CGAGCAGCGG GGCTCGCAGT GGCCAGGATC CCCGACAGTG GAATGCTGAG 720
GTTAGAACTG AAACCGCGTT TCGTGAAGTC ATCATCACGC ACGGGAAACA GGTTTGGGGT 780
GAGGGGCGGT CCAGTCCTAA GAAAGCTCTC CAGCTCCACG CGGTCACCTT CACTCACTCA 840
CCAGATGCAG ATTGCAAAGA GGCGAAACCT GTGATTTCTT TAATAATCAC AGTCTCCATC 900
TGGTGAGTGG TTAAAGTCAC GTTCCGTTTT CATTTTCCTT TTGGTGGCTG GGAAATGCTT 960
CTGATAGTAA TAGTTTTCGA TTCTGCAACT CCCATTGTCT TAGGCTCTGT AGCTCTCCAT 1020
TTTCTTCTTA TCCTTGGGAC GTGTCTTGGA CGTTTCTAAC AGGCTGTGTT CCTGGACCTG 1080
AAACTCAGCT GGAGACTGGG TCCCTTGCAG ATTTGCAGGG ACCGTCCATC GCTGGTGTGT 1140
AGATGCAAAA ACAAAACACT GGCACCACCC AGTCAGAACT GGCAGGGGCT GCCTGCACTG 1200
GGCACCAACC CCGCAGATGG CCAGGCCCAG ACCACGTGAC TGCCTGCTGG GCTCCACCCC 1260
CAACCGCAGC CCAGCCAAGG CAGAGAGGTG GCTGCACTTC CGCCGATCAG AGGTCCAGAT 1320
AGAGCTCCGT CTGCTTGCCT TGGAGTTGTT AGAAAATTAT CTTTGGGGCT AGGCATGGTG 1380
GCTCACGCCT GTAATCCCAG CACTTTGGGA AGCTGAGGTG GGCGGATCAC GAGGTCAGGA 1440
GTTCAAGACC AGCCTGGCCA TCATAGTGAA ACCCCGTCTC TACTAAAAAT ACAAAAAATT 1500
TAGCCAGATG TGGTGGCGGA CGCTTGTAAT CCCGGCTACT TGGGAGGCTG AGGCAGGACA 1560
ATCACTTGAA CCCAGGAGGC GGAGGTTGCA GTGAGCCGAG ATTGTGTCGC TGTACTCCAG 1620
CCTAGGCGAC AGAGTGAGAC TCCATCTCAA AAAAAGGTTG GGATGTCTTT TTAAGTGTGT 1680
CTGTTCCAGG AGGATGGGAA ACACTAATTT ATGATTCCAA GAACTTTCAG GGGAAATTTG 1740
TTATCCAAAC CTAAATATCT GAACACAGTG TAACCCTGGT TCTTACTAGA AGTGTTTTTT 1800
CTTAAAGAAG CTGTGAACTG GTCATACGTA CAGCGTTCAC AAGTCCCCAG 1850
|
