| Tag | Content |
|---|
EnhancerAtlas ID | HS091-18677 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:2284390-2287350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:2286042-2286061 | CTACCAGCAGAGGGAGCCC | + | 6.25 | | E2F6 | MA0471.1 | chr17:2285631-2285642 | GGGCGGGAAGA | + | 6.14 | | KLF4 | MA0039.3 | chr17:2284475-2284486 | GGAGGGTGTGG | - | 6.32 | | Klf1 | MA0493.1 | chr17:2284722-2284733 | TGGGTGTGGCT | - | 6.14 | | LMX1B | MA0703.2 | chr17:2286117-2286128 | ATTTTAATTAA | + | 6.62 | | RREB1 | MA0073.1 | chr17:2286495-2286515 | CCCCTACCCACCCCACCTCA | + | 6.13 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_00900 | chr17:2286336-2287121 | Adrenal_Gland | | SE_06238 | chr17:2282073-2285142 | Brain_Hippocampus_Middle | | SE_06238 | chr17:2285214-2287273 | Brain_Hippocampus_Middle | | SE_08501 | chr17:2280687-2285065 | Brain_Inferior_Temporal_Lobe | | SE_09633 | chr17:2286100-2287612 | CD14 | | SE_14718 | chr17:2286200-2287061 | CD4_Memory_Primary_7pool | | SE_23087 | chr17:2286375-2287174 | Colon_Crypt_1 | | SE_26563 | chr17:2286322-2286885 | Esophagus | | SE_27675 | chr17:2286344-2287517 | Fetal_Intestine | | SE_28622 | chr17:2286327-2287371 | Fetal_Intestine_Large | | SE_31449 | chr17:2286323-2287497 | Gastric | | SE_34705 | chr17:2286016-2287423 | HeLa | | SE_37443 | chr17:2282867-2285264 | HSMMtube | | SE_41748 | chr17:2286332-2287392 | LNCaP | | SE_46111 | chr17:2286267-2287244 | Osteoblasts | | SE_46721 | chr17:2286418-2286714 | Ovary | | SE_48121 | chr17:2286306-2288489 | Psoas_Muscle | | SE_51186 | chr17:2286113-2288289 | Skeletal_Muscle | | SE_52387 | chr17:2286272-2287501 | Small_Intestine | | SE_65320 | chr17:2284370-2284921 | Pancreatic_islets | | SE_65320 | chr17:2285204-2287409 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH17I002379 | chr17 | 2282971 | 2284924 | | GH17I002382 | chr17 | 2285492 | 2287823 |
|
Enhancer Sequence | TTTAAGCTCC ACAGTCGGCC AGCCCCAAAA GGCGAGGACG GCAAAAAACT AAAGTTTCCA 60
AGAGAGGTAC TCCAGCCGCC AGTCTGGAGG GTGTGGGCTG GTCAGGAAGT CAGGGTGATT 120
TGATAGCCAA ACCTCAAGTA CTCAGCGCCC TTGAGGGGAC CTCACCCCAG AGTCATGGCC 180
CCATCTCACG ATGACCAGTG GCCCCTCTAG CCTGTGGATG AGAGAAGGTC CCTGTCCCAT 240
CCCTACCCCC TGCCTGCCCT ACTGACCAGG CTGCAATGAG AAGCTGGAGC TTGACTATGC 300
CACTGCAGCT GATGGCAACG GAGCTGCCCC TGTGGGTGTG GCTCTCACCC CGAGCACTGT 360
CTGAGAGGCC GGAGGGGAGT GTCAGGAGGA GTCAGACCCT GCTGAGCTAT AGACAGGCCC 420
AGCTGTAACG GGTCTGCACC TCTCTTCCTG CCCTTCCCCA ACCCGAGTGC TACTGGTCCC 480
ATCGTCGATG GCTCCAGGGA GAAGACACCA GTCACACAAC ATGTCTTCTA CCCTAGAGGA 540
CACTGGCTTC CTGGACATTA GGGCCTGTTT TCCACTCACT CAAAGCTGAA GACCCCAGCC 600
CATGGTCCTA GCAGGCTGAA CCCAGCTTTA TTATACAGAG AGAGAGACAG ACAGATAGAC 660
AGACACAGAG TCTTGCTATC TCTCCCAGAA TGGAGTGCAA TGGTATGATC ATGGCTCACT 720
GCAGCCTTGA ACTCCTAGGC TCAAGCGATC CTCCCAACTC AGCCTCCCAA GTAGCCAGGG 780
ATGCAGGCCC CCATCATGGC AGTTTTTCTA TCTTTTTGGT AGAGGCAGAG GCTCACTGTT 840
GCTCAGGCTA GTCTTGAACT CTGGCCTCAA GCAGTCCACC CACTTGGCCT CCCGAAGTGC 900
TGGGATTACA GGCTTGAGCC ACTGCATCTG GCCCTGAACC CAGCTTTTAG GAAAGAGTGC 960
AAACTAGTGG CCAGAGCTAC CCAAAGAAAC CAGTTGGTGC AGAGAGAGCT CTGGGGCCAG 1020
GGAACTTGAT GAGCCCTTCA GGGGAACACC CCCGACCCGC CAGCCGACTC TGTTGCCTGG 1080
AGGAGTCAGA ATTCCTTTGC TGTGACCACC TAAAGGAAAT TTCACCTAGC CTGGGAGTAA 1140
CCCTTCACAC ACTTCCGTCC TGCCCTACTC CCCCTGACTA CTGGACTGGG ATCCTGGGAC 1200
CAGAGGGGAT CCCACAGCTT TTCAAAACGA TGGGACAGCT GGGGCGGGAA GAGCAAGCAG 1260
CACAGTGGGC TCTCCAAACA CCATCTCAAG GAACCTTTGC AATCTGGAAA GTCAGGTCTT 1320
CCTCTTACAG AGCAGGAGCT GGTAAATGGA AGCACCTGGA TTCATACTTT ATCCTGACCA 1380
CAGGCCCCTT TCTTATAAGC TCCAGCTGAG CCATGGGTGA GTGAGAACTG TGGGTGAGGG 1440
GGAGCTTTGA GTACAGCTTC TGCCTAAAGA TTTAGTGACA GCCCTCAGAT GACAGCCAAG 1500
TTATCACTGC CTGGGGAGGG TCTTCATCTG TGTTCCCAGT GGGCACAGGG CCTGGCACTG 1560
AGCATGCACC CAGGAAGGGT TAACCCTCAC CCTATCCCTT CCCTAAAGCG TCGCTTAGTG 1620
AGCTAATGGA AGTGACCCAG CTCTTCCAGG AGCTACCAGC AGAGGGAGCC CGCGTCTCAC 1680
AAGTAAAAAG GGCAGGCTCA GTAGGGAGGG CTGGATTCCG AACTTTCATT TTAATTAAAA 1740
AAATTTTTTT TGAGACAGAG TCTCGCTCTG TCTCCCAGGC TGGAGTGCAG TGGCGCAATC 1800
TCGGCTCACT GCAGCCTCCA CCCCCCGGGT TCAAGTGATT CTCCTGCCTC AGCCTCCTGA 1860
GTAGCTGGGA TCATAGGCAT GCACCACCAT GCCCGGCTCA TTTTTGTATT TTTAGTAGAG 1920
AAGGGTTTTT GCCATGTTGG CCAGGCTGGT CTCGAACTCC AGACCTCAGG TGATCTGCCC 1980
ACCTAAGCCT CCCGAAGTGC TGGGATTACA GGCGTGTGCC ACCGTGCCCG GCCTGAACTT 2040
TTTGAAGTCA ACTCTTCTCT TTCAGAAAAC AGGACCCAAG ACAGCACTCC CTTCCTCAAG 2100
GATAACCCCT ACCCACCCCA CCTCAGGAAG AGACGCAGAG TCAGTCTCCC CTGTGGGGAC 2160
TGGGAGTCAG TCAGGTACTG TCAGGGTGGA AATGAGAAGC TGGGCCCCCT TGCCCAGCCT 2220
GGTCTCCAGC AAGGCCTAGC TAGTGGCTCC CTGACCTCAC TTCCCACACC ACCTCCTCCC 2280
ATGACAGCCT GCCCAGGGAG AGAAGACACA GCCACAGGGA CAAGGGGCTT CCAGCCCAGC 2340
TGAGAACACG GCTCTTTGCC CCTGACCTCC AGCCTCTTCT TCCCCTTGTT CCTTTCCCTT 2400
AGAGGACAGC TTTATGGACT CCCCGGCTGA CCTGTTGTAA CTGCACCCCC AGAGCAGCCC 2460
CTCAGGAAGC TCTCACCCTC TGTGCCCAAT CCCTGGGGCA ACTCCCCTGT ACCTTTTTTA 2520
TTGGATCCGA GTCTAGGACT GGCCCCAGGT GCCACAAGGG TGGCAGATGC TGGGTAAGAA 2580
CTCTGTACCC AGTTCAGAGG TCTGACTGCA GCTCCAACGA AGTCTCCAGC TAGCCGTGTG 2640
GCCTCAACAA GTCACTGGGC CACCTCAATC CTGTTTCCTT ATCTGCCAAA ATGGGGCTAA 2700
GTCTGGCTTA TTTACTTCAC TTGGCTGTTG AAAGATGAAA CAAGATAATG CTTGTAAAAT 2760
GGTCTGAGGA AATACGAAGC TTTGCAAAAG TTTCAGACCG ACCAGAACTG CCATTTTCAG 2820
AGCGGCGGAG GCACCGGGTC AGAGCCGCTT GAGGACTATG CTGGGCAGAC AGGGTCGAGA 2880
CAGGTGATCT CACCGCTCCT GCCACATGCT TCCCTACAGG CCTCAGCCTC CTTTTGCAAT 2940
AAAATGACCC AGATGCTGCA 2960
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