| Tag | Content |
|---|
EnhancerAtlas ID | HS118-00396 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:36276160-36277630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr1:36276329-36276340 | TAATCTAATCA | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr1:36277419-36277434 | TGAACTCCTGACCTT | - | 6.04 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_09442 | chr1:36271726-36279218 | CD14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 36276711 | 36276800 | | chr1 | 36276339 | 36276448 | | chr1 | 36276339 | 36276431 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I035810 | chr1 | 36275693 | 36277127 |
|
Enhancer Sequence | TGCTTTTATG ACTATTAGCT CATTTGATCC TCTGGGAGGT AGGCAGGGCA GGTAGTTATT 60
CCATTTTACA GATGAGAAAA GTGAGGTTCA GAGAGGATGA AGTGACTTCA TTAGGGTTTC 120
AAAGGGTCAA GTGGTGAAAT AAAGACCTGA GTTTGGGTCA TTTGACTTCT AATCTAATCA 180
TCTCCTCTTC ATTAAGGCTG ACTTCATCTG TTCTATGTTG TCATATCAGT TGCCCTTTCA 240
GAGAATGCAG TTATCTGACT TTGTCACCAC ATTTTTGGGA TACCCTGAAA ATAAAACTGT 300
GGTGGTTCAT GCCTGTAATC CCAGCACTTT GGGAGGTTGA GGTGGGCGGA TCATTTGCGG 360
CCAGGAGTTC GAGACCAGCC TGGCCAGCAT GGTGAAACTC CGTCTCTACT AAAAATATAA 420
AAATTAGCTG GCTAAAAATA TAAAAATTAG CTGGGTGTGG TGGCATACCT GTAGCCCTAG 480
CTACTCTGGT GGCTGAAGTG GGAGGATGGC TTGAGCCTGC GAGGCAGAGG ATGCTGCGAG 540
CTGAGATCGC ACCTCAAAAA GAAACCCTGC CTCAAAACAA AACAAAACAA CAAAAAAAAA 600
CCAACCAAAC CACAACAAAA AAACACCTCA GGGGCTGGGC ACAGTGGCTC ACGCCTGAAA 660
TCCCAGCACT CTGGGAGGCC GAGGTGGGCG GATCACCTGA GGTTAGGAGT TCAAGACCAG 720
CCTGGCCAAC GTAGTGAAAC CCGTCTCTAC TAAAAATATA AAAATTAGAT GGGTGTGGTG 780
GTGTGCTCCT GTAGTCTGAG GCTGCTGCAG GAGAATCGCT TGAACACAGG AGGCGGAAGT 840
TGCAGTGAGC CGAGATTGCG CCACTGCACT CCAGCCTGGG TGACAGAGCA AGACTCCATC 900
CAAAAAAAAA CAAAAAAAAA AACAAAAACC AACCACCTCA GGGACCTTTG AGCACTAACT 960
ATGATTATAA CGTTTACAAA TGCAATTATA ATAGCTAACA TTTACTGAGC GTTTACTATT 1020
GCAAGGCACT ATGTTAAACG TTTTTTGTTG TTGTTGTTTT TTGAGACAGA GTCTCGCTGT 1080
GTCGCCCAGG CTGGAGTGCA GTGGCGCCAT CTCGGCTCAC TGCAGCCTCC ACCTCCCGGG 1140
TTCAAGCAGT TCTCTGCCTC AGCCTCCCGA GTAGCTGGGA TTACAGGCAC CCACCACGCC 1200
TGGCTAATTT TTGTATTTTT AGTAGAGACG GGGTTTCACC ATCTTGGCCA GGCTGGTCTT 1260
GAACTCCTGA CCTTGTGATC CACCCGCCCC GGCCTCCCAA AGTACTGGAA TTACAGACAT 1320
GAGCCACTGC ACCCAGCCTT TATGTTAAAC CTTGAATATA CATCATCTCA TGGGATAGAT 1380
GCCATTATTA TTACACACAT GCCCATTTTA TAAATGAGGA AACCGAGATG CAGAGAGGCC 1440
AAGAAACTGG CCCAACGTCA TGCAATTAGG 1470
|
