Tag | Content |
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EnhancerAtlas ID | HS113-00372 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:16507840-16512150 |
Target genes | Number: 14 | Name | Ensembl ID |
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SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arntl | MA0603.1 | chr1:16510043-16510053 | GGTCACGTGC | + | 6.02 | ELF3 | MA0640.1 | chr1:16508229-16508242 | CTACTTCCGGCTA | - | 6.25 | EWSR1-FLI1 | MA0149.1 | chr1:16508479-16508497 | GGGAGGAAGGAAGCAGAG | + | 6.42 | IRF1 | MA0050.2 | chr1:16511877-16511898 | TTTTTCTTTTTTTTTCTTTTT | + | 6.07 | Nr2f6(var.2) | MA0728.1 | chr1:16509417-16509432 | GAGGTCAGGAGTTCA | + | 6.22 | STAT1 | MA0137.3 | chr1:16511012-16511023 | TTTCCTGGAAA | - | 6.62 | Stat4 | MA0518.1 | chr1:16511009-16511023 | CCTTTTCCTGGAAA | - | 6.91 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_23091 | chr1:16507977-16509332 | Colon_Crypt_1 | SE_24743 | chr1:16508183-16508861 | Colon_Crypt_3 | SE_26540 | chr1:16504790-16512175 | Esophagus | SE_28102 | chr1:16507825-16509373 | Fetal_Intestine | SE_29455 | chr1:16507734-16509371 | Fetal_Intestine_Large | SE_31527 | chr1:16507486-16509710 | Gastric | SE_31527 | chr1:16509851-16511737 | Gastric | SE_34268 | chr1:16506936-16512113 | HCT-116 | SE_34628 | chr1:16506549-16512234 | HeLa | SE_36144 | chr1:16507720-16509431 | HMEC | SE_38062 | chr1:16507125-16509874 | HUVEC | SE_40833 | chr1:16507342-16509479 | Left_Ventricle | SE_44998 | chr1:16507356-16509449 | NHLF | SE_46140 | chr1:16507347-16510631 | Osteoblasts | SE_47009 | chr1:16508039-16509386 | Ovary | SE_47150 | chr1:16499250-16512083 | Panc1 | SE_47539 | chr1:16507961-16508560 | Pancreas | SE_47539 | chr1:16508587-16509159 | Pancreas | SE_48744 | chr1:16507441-16509527 | Right_Atrium | SE_50427 | chr1:16507395-16509522 | Sigmoid_Colon | SE_52536 | chr1:16507445-16509419 | Small_Intestine | SE_56795 | chr1:16507333-16512008 | VACO_400 | SE_57357 | chr1:16508000-16508578 | VACO_503 | SE_57357 | chr1:16508592-16509318 | VACO_503 | SE_57939 | chr1:16507977-16509011 | VACO_9m | SE_64726 | chr1:16507942-16511421 | NHEK | SE_65472 | chr1:16507356-16509554 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr1 | 16508086 | 16509162 | chr1 | 16509950 | 16510149 | chr1 | 16508402 | 16508642 | chr1 | 16510864 | 16511423 | chr1 | 16511499 | 16511858 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I016171 | chr1 | 16497941 | 16511884 |
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Enhancer Sequence | AAAGTCTTAT GCCTGTAATC CCAGCTCTTT TGGGAGGCCA AGGCGGGCAG ATCACTTGAG 60 GTCAGGAGTT CGAGACCAGC CGGGCCTACA GAGTGAAACC CCGTCTCTAC TAAAAATACA 120 AAAATTAGCT AGGTGTGGTG GTGGGCGCCT GTAATCCCAG GAGGTGGAGG TTGCAGTGAG 180 CCGAGATCGC GCCGCTGCAC TGCATCCTGG GCAACAGAGC GGGACTCCGT CTCAAAAAAA 240 AAAAAAGACT CCCGGCCAGG AAGAGAGCTT GAATGAAGTC TGACCTGCAC CAGGCCTTCT 300 GGGCCCAGAC CAGGCCTGCT TAGGGGCATG TGCCCTGCTC AGAACTTCCC CATCCCAGCT 360 AACCCAGAAG ATAGCTGGGA TGAAGATAGC TACTTCCGGC TACCAGCCCA TGATTCTTTG 420 CCAGCCTGCA CTGTTCCCTG AAGAGCAAAA AGACTTGGAA TTTCCCTGCT CTATCCAGAG 480 GGGCTGGGAT GAGGGGTCCT GAGTTCCCTT ATCCCATGTC CTACCAACCT CTGGAGCTCT 540 CCAGTCAGCC AGCTCGAGGC TCTGGCCCTA GCTGGTGGGC AATGGGAGGG AGAGGCTTGG 600 CCCAGCACCC CACCCCACAG ATCAGCCTGG TCCGGCAAGG GGAGGAAGGA AGCAGAGGCA 660 GCCTGGGCCA GCGGACACAG GGTTGGGGGT GACACAGGCC TCAGGAATTT GAAAACAAAC 720 ACTTCGCCAG GGAAGGAAGA GGCTGCTGTT GGCTGCTGAG CCCGGGCGGG CCCAGGTCCC 780 TCCCTTTCAG GGCAGGGGTG AATCCCAGTG CTGCTGACCA TGGCCCCCGG CTGGACCCAG 840 TGCTCGGGGA GTTTCCACTC CGCTGGTGGG ATGGGAAGGT CATGGGAGGT GTGGGGGGAT 900 CCAGGCTCTG TCCAGATACG GGAGCATCCT GGCTGGGGTG AGGACAGGAA GGGACAAAGA 960 GCTGGGAAAG CCACGAGACC CCAGGAGAAG GCTCAGCAGC AACAGGATGC CGCCTCAAGC 1020 ATTTATTGAG CACCCATGGT ATTCCAAAAA CTGAGAATAT AAGCACTGCC TAGCTGGGGA 1080 GATCAGGGGA AGCCTAGAGC CCTGTGGCCT TCCTGGAGGA GGTGGCATTG AACTGAGCCC 1140 TGAAAGGTAA ACTAGGACCG GGGAGGACAG AATCTTACAA GTCTCCCCCC TTCACACTCC 1200 CAGAGCCGGC GCTCAGTGAG TGCATGAGTG AGTAAGCGGC TGACCAGCGA CTATGCAGCA 1260 TGAATGAATG ACAGACTGAA TGACATGAAG CCTGGAGTCT CAAGGCCGAG ACTGCAAAAG 1320 AAGAGTCCAT CCTCCTATCC CCTCTGCTCT GAACTCTCTT CATGATCCTG AAGGTGCTTG 1380 GTACCTGGAG ACTACGGAGC CAGCCTGCCG GGGTTCTAGT CTGAACTCAG TCACTTCCCA 1440 GCTGTGTAAC TTTGGACAAG TTACTTAACC TCTCTGTGCC TCTGGTCCCT TCTCTGTAAA 1500 GTGTAGTCAT CGGCCGGGCG TGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCCA 1560 AGGCAGACGA ATCACTTGAG GTCAGGAGTT CAAGACCAGC CTGCCCAACA TGGTGAAACC 1620 CTGTCTCTAC TAAAAACACA AAAATCAGCC GGGTGTCGGG GGCAGGCACC TGTAATCCCA 1680 GCTACTCGGG AGGCTAAGGC ACGAGAATTG CTTGAACCCG GGAGGCGGAG GTTGCAGTGA 1740 GCTGACATCT CGCCACTGCA CTCCAGCCTG GGCAACAGAG TGAGACTCAA AAAAAAAAAA 1800 AAAAAATACA GAGGTAATCA TAGTGCCTCC TTCACAGGGT TTTTGAGAGG ACTGAATGAG 1860 TTTTACAAGT GAAGTGCTTA GAACGACGTT GCACATGTAG TGAGAACTAC ATGAGTGTTG 1920 GCCAATGCTA TTACTGAGGT TCCAGCTTAC GCGTTCATTG AGTCACTCAC TCACTCACTG 1980 TTCATTCACT GATTCGCTCC TACATGCCAT CCGCCACTTA CACACCCCTC CCTCTTCACC 2040 GTCATCTGTT AAGCAATCCC CGTGTGCCCG GCTCTCTCCT CTCGGTCCTC CCAGCCCCCC 2100 TTTGCCAGTC TTGGATGGTG CCCGCCGTGC TGCCAATTAC CCTAACAATT TCATTAATTC 2160 CTCTCAAGCC CAAAACAAAC AAGAAGGACC TATCTGGAGC AGGGGTCACG TGCTAAGACC 2220 AGAAGCAGGT GTGGGACAAA CCCTCTAGGA CGAGTTCTTT GACCAGAGTT CATCACCGGA 2280 GCTGCTCCAG AGATGGCCAG GCCTCCCCAC CTGCAGGTGC CCGGCCAGTG CCCCCCACCC 2340 CGGGCAGCCT CACCCACTCC CCTCTTTGAG TAAAGGTAAA GGGACTTGCC CAAGGCTGGG 2400 TTCTCCCACA TCCCGACTGC ACCTGTCCAC ATTTCAGGCT TCATTCATGC CAGGAGCCCC 2460 AGACCTGCTC CATGCACCAG CTCCGCCCAA GCCTGGAGCC CCGGGCTGGC TGAGGTGAGA 2520 GCCCCAAAGC TCGAGCCCAT TTCAGCAGCT AACAATTAGA GCTGGTGTGA ACATGATGAC 2580 TGCATGCTGA TTAATGTAAG ATGGCTGAGC AGAAGATCCC GCCATTTCCT TCCCCACAGG 2640 CCCTGGGAGA ACAGGTCCCG CTGGGGAAGA CTCTGTCGTG TTCTGCAAAA GCCATTTCTT 2700 GAGCACGTCC TGCAGGCCGG GCACTGCGCT GGGCACTTGA TTCCTTTCAA CAGCATGACA 2760 TGGTGGGAGG ACAACTTGCC TCTCATTGAT GAAGAAACGG AGGCTCAGAG AGGTAAAGGA 2820 ACTTGCCCAA GGCCACACAG CCAGTCAGTG TGGTCCTGGA ATTCCAATCC AGGTCTTCTC 2880 TTGCTGATTC CTACCCCCAG GGATGAGCCA GTTTGACATT TGTGGAACTG GAGAGAGGCT 2940 GGGTTTGGGC ATAAGGTAAT GTTTAGGCCA GAGGGTGGAG AAGGAGAGGA CAGCCAGAGA 3000 GGCAGAGCCA AGCGCCAGGC AGGAACAATG GTACAGGGCA GGTAACGGGA GCCCGGCCAG 3060 CTCTGGGACT CCTGGGCAGG CCCTGCTGGG CCCTGCGAGC AACAGGCTCA CCCTGTGGAG 3120 CTGCCAGGGT GACAGCAGCC TCGATCTGCT GACTCAACGA GTGCATCGGC CTTTTCCTGG 3180 AAAACAGTAG ACGCAGTGTG GGTGTCGGAG GGAGGCACCT GTTTGGGAAA AGGGTGTGTG 3240 GGAACCCTGT CCTGCCCTGC AGCTCCCCAC AGCCAGTGTA CAGGTACTTA GCTCCAGGTG 3300 CCCCCCGAAC CTCCCACCAC CTGCCCAGAC CCCAGAAGCC ACCGGATCCA GGAGTCCGAG 3360 CCAGCTGTGG GCTGAGTCCA TGGTGCCACC AAGGCTCTGC ATGACCAGTG CTGCCAGCCA 3420 CCACCTCAGC CAAGCAGCAC AGCCTCTCAG GGCATGTCCC CACTTGCTGT CTGCAGAGCC 3480 TTGTTTTGCC CCACCCTGAA GGGGCAGGTG TAGACGAGCA TTGAGGCAGG TCTATGTGAC 3540 ACCACTTGCT GTCACTCTTC TTTGGGAGGT ATCAGGGCCA CTCTGCCACG GGGCACAGCT 3600 TAGGGCCTCC ATGGAATCTG GTCTGAAGGA TCCCGCTGCC CAGAGGGGGG TCAAGAATAC 3660 GGAATGGGTT CAGGAGCACC CCCTGTCTTC AGGATCCAGT TGGGGGAGGT CCCAGCAGGG 3720 CCAGTCACAG ACACTTGTCA CACCCTGGAG GGGATAATAG GATCTGGGGC TCAGCCTCCA 3780 CCAATTTCAT CACCACACAC CACACCCAGG CAAGGGAGAG CAGAGGCATC AGCAGGGCCT 3840 GGCTGAGGGG CTGAAGCCTG GTGGGGAAGC AGGGAGGGCC CCTGGGCCTC TCGGTCCTAT 3900 CTCTTCCCAA TCCAGGCCTC AGCGGACTCC AGGGCAGGGG TGCGGGAGCT GATTTCCAGG 3960 TGCAATATTC ACTGTCACCA TGGCCGCTTC CAGCACCCAG CCTGAATTTC CTAGTGCAAT 4020 GCTGGGAAGA ACTAGTCTTT TTCTTTTTTT TTCTTTTTTT CTTTTTTTTT TTTTTTGAGA 4080 CAAACTCCTG CACTGTCGCC CAGACTGGAG TGCAGTGGCA CGATCTCAGC TTGCTGCAAC 4140 CTTCGACTCC CAGGTTCAAG CGATTCTCTT ACCTCGGCCT CCCAAGTAGC TGGGATTACC 4200 AGTGCCCCAC CACCACGCCT GGCTAATATT TTTTTTTTTT TTTTTTTTGA GACGGAGTCT 4260 TGCTCTGTCA CTGAGGCTGG AGTGCAGTGG CGCGATCTCA GCTCACTGCA 4310
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