| Tag | Content |
|---|
EnhancerAtlas ID | HS091-12342 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:20886580-20888420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr14:20886597-20886607 | GCTAATCCCC | + | 6.02 | | HNF4G | MA0484.1 | chr14:20886807-20886822 | TGGACTTTGAACTGG | - | 6.25 | | Hnf4a | MA0114.3 | chr14:20886805-20886821 | GATGGACTTTGAACTG | - | 6.35 | | MNX1 | MA0707.1 | chr14:20887526-20887536 | GGTAATTAAA | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr14:20888337-20888352 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28028 | chr14:20879130-20888428 | Fetal_Intestine | | SE_29051 | chr14:20879173-20888453 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 20887800 | 20887916 | | chr14 | 20887445 | 20888020 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I020414 | chr14 | 20883069 | 20888349 |
|
Enhancer Sequence | TTGATCAACA AACATCTGCT AATCCCCTGT CAAAGAATAG TGCTAGTACA TGGGTAAAAT 60
GTATACAACA TGCCTTCTTC TCAAGACTTC ATCATCTTGT AGAGATAGAC ACATGTAGAA 120
ATCACAAAAA TACAAGGCAG ATAAAGAGAA GTGCTATAAT GGACTAAGAG ACAAACTATA 180
GGGTTATATA GGTGAGAGCA AGGATCTCAA GCAACTCCCT GGAGAGATGG ACTTTGAACT 240
GGGAAGGGCA GGCCTCTGAT AAGCTGGGAG GGGAGTGACC AGTAGGAAGT GGAAAGGCCA 300
TTGGTTTTAC CTGATTTTTT TCTTCTTTGT GAATGATTAC CTTTAGATTC ACAGTATACG 360
TTTGTTTGAC CTAACCATCA CAACTTAAAG CATCACACAA GCCGTGATAT GTGGACAAGC 420
ACACACTTAC TGGATAGCCA CTTGTCACCT CAGACAAGCC CTTCTGGGCC ATCTGAAAGC 480
AGATTACAAG AACCTCAGTG TCTTCTCCCT TCTGACTCTT CTGAATCAAA ACAACCCTGC 540
ATTTGGCCTC TGGTCTGTGG ACATTTGCCA ATATCTTTCT TCATCTTTCT TTTTTTTTTC 600
TTTTTGAGGC AGAGTCTTGC TGTGTCGCCC AGGCTGGAGT GCAGTGGCAC GATGTCGGTT 660
CACTACAACC TCTGCCTCCT GGGTTCAAGC AATTCTCCTG CCTCAGCCTC CCAAGTAGCT 720
GGGATTACAG GCACCCACCG CCATGCCCAG CTCATTGTTT GTATTTTTAG TAGAGACAAG 780
GTTTCACCAT CTTGGCCAGG CTGGTCTCAA ACTCCTGACC TCAGGTGATC CGCCCACCTC 840
AACTTCCCAA ACTGCTGGGA TTACAGACAT GAGCCACCAT GCCCGACCTC TTTCTTCATC 900
TTTCTTCAAG GACATTCCTC ACTGACTAGT CTCCCTAATC GGGTATGGTA ATTAAAATAG 960
GCCACAAATT CTTTGCTTCC TCTCCCATTG AGAGGCAGAG TCTAATTCCT TCTTGAAACT 1020
GGGCTGACCT GGTCACTTGC TTGACCAATA TAATGTGGCA GCAGTTGCAT TCTGGGACTT 1080
CTGAAGCTAG GTCAAAGGAA ACTTGCACTT CCTCCAGGAC TCTGGAACAC TCCCTTGGGA 1140
AGCCCTGAGC TGCCATGTGA GTCCAACTAC CGTAAGACTG CCACTCTAAA GAGGCCACAT 1200
GTAGGTGTTT CAATTAACAC ACTCAACTGA GCTCAGCCTT CTAGCCATCT CCACCAGGGC 1260
ACCAGACATG TGCCCTGTCT GGTGCCCTAG TGGAGAAAGA AGCAGTCTTA AGTCCCTCAG 1320
ACCAGTTCAT CTACCAATTG TCTATTATCA AGTAACTTCC ACTAATGACA CATGAAACAG 1380
AAGAATCATC TAGTGGAAGC CTGCCTAAAT TTAGTGAAGT CAGTTACACA TAAAATTGTG 1440
AGATATGATT AAATGGTTGT TGTTTTAAGT CACAAAGTTT TGGGCAGCAA ATGATAACTG 1500
GTACACTAGG CCTGCAAAAC ATAAGACAGT TTACATCAGG GTACTCTGTA ATCATCCTAC 1560
TTTTTTTTTT TTTTTTTTTT TGAGACAAAA ACAGTACACC TGATCCCGAA AAGGATTTGA 1620
GTCCTGCTTT TGGATGGGAT GAGGCAGAGG TAATTGGAAG TAAACTTTGG ATCTCAAAAT 1680
AGTGAACTTG GTGCCGGGCA CAGTGGCTCA CACCTGTAAT GCCAGCACTT TGGAAGGCAG 1740
AGGCAGGCAG ATCACCTGAG GTCAGGAGTT CAAGACCAGC CTGGCCAACA TGGTAAAACC 1800
TCGTCTGTAC TAAAAATACA AAATTAGCCG GGTGTGGGGG 1840
|
