| Tag | Content |
|---|
EnhancerAtlas ID | HS091-21429 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:77975610-77977760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr17:77976538-77976553 | AAAGACCAAAGTCCA | + | 7.03 | | ZIC1 | MA0696.1 | chr17:77976492-77976506 | GGCCTCCCGCTGTG | + | 6.16 | | ZIC3 | MA0697.1 | chr17:77976492-77976507 | GGCCTCCCGCTGTGA | + | 6.14 | | ZIC4 | MA0751.1 | chr17:77976492-77976507 | GGCCTCCCGCTGTGA | + | 6.03 | | ZNF263 | MA0528.1 | chr17:77975642-77975663 | CCACCCCCCGCCTCCTGCTCC | - | 6.15 | | ZNF263 | MA0528.1 | chr17:77975636-77975657 | TTCCCTCCACCCCCCGCCTCC | - | 6 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27830 | chr17:77975391-77977724 | Fetal_Intestine | | SE_28735 | chr17:77975584-77977926 | Fetal_Intestine_Large |
|
| | 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 |
| GH17I080001 | chr17 | 77975678 | 77977566 |
|
Enhancer Sequence | CTTGCCCTGG ACCCTCTCAC ATGCCCTTCC CTCCACCCCC CGCCTCCTGC TCCCTTCCTC 60
ATCCCCTGCT TTGTGTCCCC GTCTCCTGCT CCAGGCTCTG ATTTGCTGGG CAGCTGCTGC 120
GCCCCGGAAC AAAGACGGGA AGGGCAAAGT GTGTCCTGAT TCGTGTGCCA CCGCTCACTT 180
CTTCGCCCAC CTCCAGGAGT TTCTAATCCT CCTCGGGCTT GCCTGGAGGG TTGGGCAGAA 240
AAGGAACGGC AGGAAACGCA GAAGGGATCC GGAACGAGCA GAGCTTTGTG AGTCCAGGGC 300
GACACCCCCA GGGCCTTCCG TGGGAGCTCC TGCAAGGATG CTTCCCAGCA CTGGGTCCTG 360
GCCCACCAAG CGCACTGGCT CTAGCTCATT CTCAGAGACT GGACTCTTCC CCGAGAGCCT 420
CATTTCTGTC CTCTGTGCCG TGTAGGAGGA CAGGGGCCAT TACACCAACG ATGAACGATA 480
ACGCCGTTAA TAATTCAGCC GCTGCCGCTG ATACTCGGTC GACAAGGAGC CTTTTCCTCC 540
TAAAGGCAGA AAGCACTTAG ATGCCGTTTA TTACTGCCTC GCACGCCCTG CGGGGTGGGC 600
TGGCACCTGC CAGGGAAGCC ATGTGAGGTG GGGAGCGGCC GCCCCATGGG GTCTGCTGTC 660
CAAGCACTGG CCAGCTCCAG GTGAACCCTT GTGCCATCGC CCCCATGACA GGGGCCACCC 720
TGAGGGAGTA GAGGGGCCTT GTCTTATCAT CTCGTCTTTC CCCCATTACT TTGGACAGAG 780
AGTTTTTCGG GCCTGTCCTG CTGGGAGGGT CGCTACGTTT CTAGGGTCCA CCTTCCATCC 840
TCCCAGGAAC ATTCCGTCCA GACCTGTGCT GTCAGGCATG GAGGCCTCCC GCTGTGACCA 900
CCAAACTTCA CATTCATTGA AGATAAAGAA AGACCAAAGT CCAGTTGCTT GGCCACATCT 960
GCTGCATTTC TAGGGCGTGG TGGCCACACA CAGTGGGGCA CAGGCACAGG ACCGCGTGCA 1020
CTGCAGGACG CTCTGCTGAC GGCGCTGGCC CAGGCACTGG GAGGACCCTG TGAGGAAGCA 1080
CCCGGGAACG GTGGCGCACG TAGGGAACAC CACGCGGCCT TGATAGGAGC TCTCCAGAGA 1140
GAAAGCTCAG GTCCCAGCAG GGGTCACGGA GAAGAAAGTC TCTTCCACCT GCAGGTGGGC 1200
TGGGGATTCA GCAGGAGAGA GGAGAACATT CCAGCTGCGG GCAGCAAGGT GGGAAGCGGC 1260
TATGCTTGGG GTGAAGTGCC CAGTGTGTGT GCAGGAAAGG GCAAGAGGAA AGTGGGAGGG 1320
CAGGGGGTCC CGGCAGCACC CCCAGGTGGG CAGCACATTG CTCCTGGCCC TTGCCCACCT 1380
GTGGCCGCGC CAACCCGCTT GGACTGAGTC TGACCTGGCA GGAACTGCAT GACAGAAACC 1440
ACAGTAACAA GTGGCCAAAC TCTGAGGCCA GGCCACCCAG CCCATCCCAA CACCCAAACA 1500
CCATCTTGCC TAGGCTGGCC ACCCCGGGAA CGCATGCCGG GAATGACAAG AGGACCCAGG 1560
GAGAGAGAGA ACGAAACACT CACTTCCCCA GGGGGAGGCC CCGCTGGCGG CACGGGACCC 1620
AAGGTGGCAG GCCGGCGGCA CTGGTGTCAC TGGAAGGACC TCAGTGACCA GCTCGCCCTG 1680
GAGGCCTCTT CACTAGTTAG CAGCGTGCAG CGCAGTGGGA GATGCTTAGC GTCCCCAAAT 1740
GTGCAGGTTC TCCCCTTCTG TCTATTTTTA TACATTGGTT TTCATTCTAA GCTTAATATA 1800
ATCACAGAAT AACATTTTTG AAAACAGAAA AGTAAAAAAA AAAAAAAAGT GCTCATAATC 1860
ACACTAGGCT AACACGTGGG CACACCTTCC TCTCAACCTC TGCCATCCAC TGCCGTGGCC 1920
ACTGACCACA GGCGCTATCC ACATTTATAT TCATCAGGGC CGGGCACGCG GCTCATGCCT 1980
GTAATCCCAG CACTTTGGGA GGTCCAGGCA GGAGGGTCAC TTGAGCCTAG GAGTTTGAGA 2040
CCAGCCTAGG CAACAGAGCA AGAGTCTGTC TCTAAAAAAT AAAATAAATG AACGGGGCAT 2100
GGTGGTGCAT GTCTGCAATC CCAGCTACTT GAGAGGCTGA GGTGGGAGGA 2150
|
