| Tag | Content |
|---|
EnhancerAtlas ID | HS118-05503 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr13:99708930-99711080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr13:99709794-99709805 | TGTTGTGCAAT | - | 6.14 | | Nr2f6(var.2) | MA0728.1 | chr13:99710634-99710649 | TGAACTCCTGACCTC | - | 6.22 | | RREB1 | MA0073.1 | chr13:99710890-99710910 | CCCCCATCCACCCTCACCCA | + | 6.43 | | SREBF1 | MA0595.1 | chr13:99710376-99710386 | GTGGGGTGAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26943 | chr13:99708734-99709689 | Esophagus | | SE_26943 | chr13:99710446-99711821 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 99709435 | 99709532 | | chr13 | 99709670 | 99709847 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH13I099056 | chr13 | 99708863 | 99709850 | | GH13I099058 | chr13 | 99710447 | 99711821 |
|
Enhancer Sequence | CTGCTGGGGT GGCTGCCCGG CACCTCCCTT TCCCTGTAAC GTGTTGTTTT TCTGAGATGT 60
CCTCTTTCCC TTCCCCCAGT GGCAATCAGG GTCATTCATG CCAGGTCTGA TGCAAGGCCC 120
CCCAGGACAG GCCTTCCCTG GAGGCCAAGG AGCAGCTCCT CGCCCTGAGG AAAGACAGTG 180
GCCCTGAGGA GCCATGCGTA CAGCAGCGGG GATCCGAGAA GCCACATTCC TACAGATGAC 240
CCCATGACTT GGTATCGGAC CCAATGTGGA TCACCTCCCT GGGGGATTAG AGCAGCCTGA 300
GAGAAGGACC AGTTTCTTGC CAAGTAGCTG GTCTCTCAGA CAGCGAATTC CTACCATGTA 360
GACTAGAAGC AAAGAAAGTC AATCTCCAGG CAGAGGACCC AAAAACTCTA GAGAGCAGCC 420
GAGATAAGAG AGGATCTTGA AGGCTGGGAC CCCCTCAATA CACTCAGCTG GACCCCCACC 480
CTTTAGTTCT TGGAGACATA CTGTGTCCTT ACAACATATA TCCCTTTTTT CCTTTAATTA 540
CTTGGAATGA GTTTCTGTCA CTTGCAACCA AGAGTCCAAA TTAACACATC TAATTCCTAG 600
CATACAGACA AGAAAAAATA AGTAGTAGTC TCAAAATGTT ACGAGTTGAC ATATTGGGCC 660
TGAAATCTTA CAGCACAAAA CAGGTAACCA CTGAATAGGG GGAAAATGGT ATTCTTAAAT 720
CTTAATTTTG AGACAATTAC CCTGCCACTA AGGCACGGTA AGTCCTGGGT GAGCTGAGGA 780
CCAGATCTTC ATTGCGCCTC TGATTTCTTT ACTAAGCCAC TGACTCAGGG ACAACCTTGC 840
ATTTGGAGGA TTTCCACATC TTGCTGTTGT GCAATATTTC CCAAATAAAA GAATAATATT 900
TAACACCTAA AGGTTTCCAT AACACTGATT TGCTGCTTTA AAAAAGAAAA AGCAAATGCA 960
ACTTATAAAG ATTAAAAATA CAAATTATAA ATTTACAAGT GGAACAGCTT CAAAGCTGTT 1020
TGAAACAATA ACAATCCCTT CCTTAAAGAA AAGCAATTTC AAAAGCATAG ATAAGCAATC 1080
CAGGAGTGCC ACACCAGCTT ACAACACAGA GATCAGCAGG CACTCGCCTT GGACAGTAAA 1140
CTAATTGACA CACATTTAAC TGAGTTTGAA CATACTGTCA TTCCCATTTA TTTTTCTTAT 1200
ACTGATAATA CACTGTAATA ATACACTGTA ATTCTGTTAT GTTGAAAACT GATTGTATAC 1260
TGATTGAGAC CTAGATTTAC AATCCTAGAA TAATTACATA ACTTTTATTA GACAATATTT 1320
CAAAAGGCAA AAGACGGCCA AAACAGAGGG GGAAGGGTAT TTATACAATA TCTCTCTCAA 1380
ACTGTACATG ACCAACAAAC CAAGAAAAAT ATGAAATGTC CCAACTTCAA AAACACCCAG 1440
GCCTGGGTGG GGTGATTCTG ACCCACAGTG TACTAACAGT ACTTGATATC TTTTTTTTTT 1500
TTTTTTGAGA TGGAGTCTCA CTCTGTCACC CAGGCTGGAG TGCAGCAGCA CCATCTCAGC 1560
TCACTGCAAC CTCCGCCACC CAGGTTCAAG TGATTCTCCT GCCTCGGCCT CCTGAATAGC 1620
TAGGATTACA GGCATGCGTC ACCACACCCA GCCAATTTTT GTATTTTTAG TAGAGGTGTT 1680
TCACCATGTT GGCCAGCCTG GTCTTGAACT CCTGACCTCA AGTGATCCGC CCACCTCGGC 1740
CTCCCCAAGT GCTGGGATTA TGGGCATGAG CCACTGCACC TGGCCAAGAG TACTTGATAT 1800
CTTGATACAA ACAGTGCCAG GGGCCACAGA GCACAGTGAA GAACCAGATG AGACATCTGC 1860
TTGTGTCAGC AGGTCCCAGG ACCCCCTGCC CTAATGCTGC ACCTCTTCCC TCATCCTGCT 1920
CTATGTGCCC CATAGAGCCA GGGCCATTTA CCAAGGGTTC CCCCCATCCA CCCTCACCCA 1980
GTGGAGGCCT GGAAGCACCT GGTATGCTCA AATAAGGCCA CACTGTAGAA GGTAACAGAG 2040
CCAAGGAAGG CAGGCTGGGT CATGCTGCCC TTCAAGCACT GCAAGGACTC CACCCCCTAA 2100
AGCACTCATA GGGCACATGT AGCAGCCACA CACGAGCCCT GCTTTGGGGA 2150
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