Tag | Content |
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EnhancerAtlas ID | HS091-41005 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr6:36647900-36651870 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr6:36650184-36650199 | TGGCCTTTGGCCTTT | - | 7.21 | IRF1 | MA0050.2 | chr6:36649099-36649120 | TCTTTCTTTCTTTTTCTTTCT | + | 6.14 | IRF1 | MA0050.2 | chr6:36649117-36649138 | TCTTTCTTTCTTTTTCTTTCT | + | 6.14 | IRF1 | MA0050.2 | chr6:36649043-36649064 | TCTTTCTTTCTTTTTTTCTTT | + | 6.34 | IRF1 | MA0050.2 | chr6:36649180-36649201 | TCTTCCTTTCTCTTTCTCTCT | + | 6.62 | IRF1 | MA0050.2 | chr6:36649198-36649219 | TCTTTCTTTCTCTTTCTCTCT | + | 6.86 | IRF1 | MA0050.2 | chr6:36649121-36649142 | TCTTTCTTTTTCTTTCTTTTC | + | 6 | NFIC | MA0161.2 | chr6:36651361-36651372 | TACTTGGCAGA | + | 6.62 | REST | MA0138.2 | chr6:36650144-36650165 | GGCTCTGTCCACTGTACTGGG | - | 6.23 | TP63 | MA0525.2 | chr6:36650420-36650438 | TGCAAGTTGGGACTTGTC | + | 6.5 | ZNF263 | MA0528.1 | chr6:36648223-36648244 | CTCCCATTCTCCCCCTCCCCA | - | 6.16 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_09785 | chr6:36644753-36649240 | CD14 | SE_09785 | chr6:36649543-36655272 | CD14 | SE_10510 | chr6:36645365-36652556 | CD19_Primary | SE_11108 | chr6:36644576-36654928 | CD20 | SE_25216 | chr6:36646088-36648729 | Colon_Crypt_3 | SE_25216 | chr6:36650066-36651389 | Colon_Crypt_3 | SE_27338 | chr6:36644739-36649067 | Esophagus | SE_27338 | chr6:36649190-36651696 | Esophagus | SE_29503 | chr6:36643673-36649366 | Fetal_Intestine_Large | SE_29503 | chr6:36649488-36651835 | Fetal_Intestine_Large | SE_32367 | chr6:36644740-36649022 | Gastric | SE_32367 | chr6:36649551-36652319 | Gastric | SE_36489 | chr6:36643467-36652175 | HMEC | SE_37550 | chr6:36642176-36651633 | HSMMtube | SE_45438 | chr6:36643583-36649198 | NHLF | SE_45438 | chr6:36650042-36650751 | NHLF | SE_46998 | chr6:36646007-36648502 | Ovary | SE_47969 | chr6:36646369-36648535 | Pancreas | SE_47969 | chr6:36650039-36650989 | Pancreas | SE_53210 | chr6:36644780-36649059 | Small_Intestine | SE_53210 | chr6:36649506-36651969 | Small_Intestine | SE_59249 | chr6:36634013-36660855 | Ly3 | SE_64792 | chr6:36643535-36649399 | NHEK | SE_64792 | chr6:36649495-36652124 | NHEK | SE_65645 | chr6:36644736-36652645 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GCAGCTTCCC CTCTCCTTGC CTCCCTCCAC GTCGCGTTTC TGGGAGGACT TGCGAGCGGT 60 TTTGTTTTCG TTGCTCCCGT CTATTTTTAT TTTCCAGGGA TCTGACTCAT CCCGTGCTTT 120 GGGCGTGGAG ATAAGGTGGA GGGGCCGGCT CCCGGCGCGC GCGCGCGTGC GTGTCTGCGC 180 GGGCGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTCTGTGTCA GAGACGGCAC 240 AAGAGCGCGC GGTTTCCCAA CAGCGGCGGG AGTTTCGGAA GCCTGGCCGG CTCAGCGTGA 300 CGTGTTCGCG GCCCCCCGGT CCCCTCCCAT TCTCCCCCTC CCCACCCCAG GGTGACGCGC 360 AGCCGGAGTG GAAGCAGTTT TGGCGGGCGA GCAGCGCCTT GCAGGAAACT GACTCATCAC 420 TACTCCCTCC AGCGGTCCGA GGCTCTGCCC ACGCACCTCC CACTCCGCGC GTGATTTCCT 480 GGAGGCCGGC GCCCCCTCCC GGCCCTGGCG GGAATAGCAC ACAGGCTTTC CCGCGGAGTG 540 GGGCTGGCCG GCGCGAACCG CCGCGGCTAC TCCTGGGCTC ATCCGAGATC AACCCCTATG 600 CCATTACCAC CCCTTCAAAG GAGCACTCCT TAGGTTCAAC AGTATTCACT GAGCTCTTAC 660 TGGAAATTAA AATATGGCTG AAGTCTAAGG CAGGAAGGCC AATAAAGGAG GCTATTTTTA 720 ATTGTTTCTA AAACAAGGGT TTGCGTTTCT GAGTTTTCTT TGGGCTGAAA GTTATTATGA 780 GCATGAGAGC AGATTTTGAT GGGGGAGGAG AGGCCTATGA GAGCCATAAG AGAAGGAGGG 840 GTGGTAGAAG AGGAGAGGGT GCCTGCCTAG ATCCTAGTCC TGTCTTGAAC TCCCGAGAGC 900 CAGGGAATAT CCAGCACCTT GATGAAGCCC TAGGCGGGCG CCTCCTCCTT GTGCCTATGA 960 TGTATTGAGA CCCAGAATGT CCATTTCAAA CATACCAGTG TGTCTCCGCT TGGCTGGCAA 1020 CCCAAGAGTG CCCATCTGAG GAATTGTGCC AAACACTTGC TTGAATCTTC AATCTGGATT 1080 AAGTTGGTCT CGGGAGGCAG GGCCTCAGCA ATCTATATTT TGAAAAAACT CCCTAGGTGC 1140 TTTTCTTTCT TTCTTTTTTT CTTTCTTTCT TTCTTTCTTT CTTTCTTTCT TTCTTTCTTT 1200 CTTTCTTTCT TTTTCTTTCT TTCTTTCTTT TTCTTTCTTT TCTTTCTTTC TTTCTTTCTT 1260 TCTTTCTTTC TTTCTTTCTT TCTTCCTTTC TCTTTCTCTC TTTCTTTCTC TTTCTCTCTT 1320 TCTTTCTTTT CTTTCGACAG AGTTGCACTC TGTCACCCAG GCTGGAGTGC AATGGCACCA 1380 TCCTGGACTC AAGTAGTCCT CCTGTTTCAG CCTCCCAAGT AACCGGGACC ACAGGCGTGA 1440 TCCCCCCGCC CCCATGCCCA GATTTTTTTT TTTTTTTTTT TTTTTTTGAG ATGCGGTCTC 1500 GCTCTGTCAC CCAGGCTGGA GTGCAGTGGC GTGATCTCGG CTCACTGCAA GCTCCGCCTC 1560 CCGGGTTCAC GCCATTCTCC TGCCTCAGCC TCCCGAGTAG CTGGGACTAC AGGTGCTGCC 1620 ATCATGCCCG GCTAATTTTT TTTTGTATTT TTAGTAGAGA CGGGGTTTCA CCGTGTTAGC 1680 CAGGATGGTC TCAATCTCCT GACCTCGTGC TCCGCCCTCC TCGGCCTCCC AAAGTGCTGG 1740 GATTACAGGT GTGAGACACT GCACCCAACC ACCCAGCTAA TTTTTATTTA TTTTTATTTT 1800 TAGTAGAGAC AGGGTCTCAG CTAGTTGCCC AGGCTAGTCT TGGACCCTTG GGCTCAAATG 1860 ATTCTCCCAC CTCTGCCTCC CAGAGTATTA GGATTACAGG CATAAGCCAC TGCCCCTGGC 1920 CTCCCCAAGT GATTGTGATG GGCCTCTCTG GTTAAGAAAC CTCAAAATTA GAGAGGGAGT 1980 GGGGTTCAAT ACTACAGCAC AGGACTCAGG GCAAACAGGC CTGGGTTCAG ATCCTGGCTG 2040 TGCCACTTAT GAACTGTGTG ATGTTAGGCA AGTTACTTAA CTTATCTGAG CCTTGGTTGC 2100 CTCTTCTGTA AAAAGGGAGC TAATAGATAT CCACTTTTTA GGAGGATTGA TATTTTTAAA 2160 CTGCTTAGAA CAGCCCCCAA ACATAAAAAT ATATAAATAA ATCCCAACTC ATGCCTAGCA 2220 GAGGGTGGAT AGAGGTTATT TGAGGGCTCT GTCCACTGTA CTGGGTGACC CCTTTATGGG 2280 GCAGTGGCCT TTGGCCTTTT TAGCTGTATG ACTCAGGGGC AAGTCTCATA TCTCTTCCAT 2340 CTCCTGCCCT TTAAACTTGG TGTGAAGTTA CCAAGAGCCT CCTCTCCCAA CCAGCTGGGA 2400 CGTGAAACTG TGGGCTCCAC TGATCACAAG CAGTGGGGTG AGGTGGGGTG GAGCAGATGT 2460 GGCATGTGTC CCGGGCTTCC TGCCTCATGA GGACTCAGCA GAGCTTTCAC CCCCAGAAAC 2520 TGCAAGTTGG GACTTGTCCC TAGGAAAATC CAGTTGCTGC CAAGGTCGTG CAGTCACTCA 2580 GCCCTGGAGT CAAGCCAGAG CAGGCAGGTA GGTGCCAGGG CTCCCTCATG GGCAAACTCA 2640 CTCTCCGTTT TCCCTCTCCT GAAGGGGGAG GAGAGGAGCC AGGTAGACCA GCCACCTTTA 2700 ATTTTCTTTT TGCCTGCAAA ACGGTTTCCT TGGACACAGG CAACACGAGG CAGGGGCTGC 2760 CAGGTGTCTA GACTTCAGAT CACCTGATGT GCCTGGCAGG ATGTGGCTCA GCCTGGGAGA 2820 AATCATCCCT TGCGCTGCCC CGCCCGGCCC CTCCTTACCC CTAGGCCACC CGCCTGACGA 2880 CATCCTTGGG AAAGGCCCTC AGCCTACAGC ACCTGTCAGC TGCTGTCTGA AGGAGGTAGT 2940 TGGCAGGGGG AAGTGATAGG GGGGAGGCTC AGTAAAACTG AAGGCAGAGA GGAATAATCA 3000 TACTTCTGTT TTCAATGCAC TTCTCTATAC GAAGTGCTGC TGGCACGTTA CCTACATTAA 3060 CTCAGTTAAT TCTCATGTCT ATCCTCTGAG ACAGTCACTA TTACTATCCC CATTTTATAG 3120 ATGAGGAAAC TAGAGCTCAG ACAAGTTAAG TTGCTTGCCC AGGGTCACCT AGTAAAACCT 3180 GGACTCCAGC CCAGGTGATC TGGCTCCAGA GCCCTCCTGC TTAACCACCA GGATACAGCC 3240 TTTCATTCAG CTCTGTTCTG TCTGCCTTGC TGCATGGACT CTGTGATCAA TTTCTTGAGT 3300 ATGTGTCTGT AGCCATGCTC TTTAAACTTG TACATGGCCC CATTTATGGA TGAGGAAACT 3360 GAGACCTAGA GACATTAAGT GGCTTTTTAA AGCTTACGTA GTAACTGGCA GAGCTAGGAC 3420 CACAACCCGG GTGCTTTTTG CCCCAAAGTC CCGGGTACTT TTACTTGGCA GAGCAGGGTT 3480 ACCCTACTTG GGGATCTGGG TCGGGGGACT TAGGAGGCTG GAGGAACTGT CAGACTGTTT 3540 CTTCTTTTGG GAATTGACCT TCTGGCCAGG GCTGCGATTA GGAAACTGCT GGACTCTGGC 3600 AATTCACACA TATTTGGGGG GCATTCACAC CCATGAGGGA CACCTCTGGG GGGAAAACAA 3660 ATTGATTTTA GCTGATAATA CCTGGTGGCA AACAGGACCC TGGTCCTTGC TCTTGCAATA 3720 GACTTGCCTT TGTTGACATT AGCTTGCCCT TCAGTTGCCT GCTCTCCCAG TGACCTTGGT 3780 GTGCCAGGCT GGCTGAGCTC TGCTGGTGGG GGTCAGGCCT CCTGTGGGAA GGAAGCAGGA 3840 AGACCAGCTG GAAGGAGTGA GAGAGACCCT CTGGTAGGAA GACGTCACCT GAGGTGACAC 3900 AGCAAAGCCC GGCCAGGTAA CATAGTGTCT AATCTCCGCC GTGACCAGGG CCTTCCTTGT 3960 ATCTCTGCTG 3970
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