Tag | Content |
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EnhancerAtlas ID | HS113-02389 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:154398830-154401670 |
Target genes | |
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) |
IRF1 | MA0050.2 | chr1:154399000-154399021 | AAAAAAAAAAAGAAAGAAAAG | - | 6.41 | POU2F2 | MA0507.1 | chr1:154399204-154399217 | TGAATTTGCATGT | + | 6.05 | TCF7L2 | MA0523.1 | chr1:154400148-154400162 | CCCCTTTGATGTCT | - | 6.14 | ZNF263 | MA0528.1 | chr1:154401281-154401302 | TGAGGAGGAGAGCGAGGGGAG | + | 6.42 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00437 | chr1:154399481-154401751 | Adipose_Nuclei | SE_01040 | chr1:154399528-154400582 | Adrenal_Gland | SE_01040 | chr1:154400681-154401626 | Adrenal_Gland | SE_06653 | chr1:154399347-154403450 | Brain_Hippocampus_Middle | SE_09189 | chr1:154398672-154408855 | CD14 | SE_16173 | chr1:154399945-154400671 | CD4_Naive_Primary_7pool | SE_18405 | chr1:154399517-154407766 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19165 | chr1:154401205-154402489 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_24531 | chr1:154399580-154400359 | Colon_Crypt_2 | SE_26130 | chr1:154399302-154401704 | Duodenum_Smooth_Muscle | SE_26877 | chr1:154399516-154400662 | Esophagus | SE_26877 | chr1:154400694-154402391 | Esophagus | SE_32086 | chr1:154399571-154400607 | Gastric | SE_32086 | chr1:154400656-154401897 | Gastric | SE_41139 | chr1:154399325-154402156 | Left_Ventricle | SE_41647 | chr1:154399531-154400535 | LNCaP | SE_41647 | chr1:154400745-154403911 | LNCaP | SE_42431 | chr1:154399355-154400656 | Lung | SE_42431 | chr1:154400696-154402137 | Lung | SE_47983 | chr1:154399591-154400258 | Pancreas | SE_47983 | chr1:154400922-154401243 | Pancreas | SE_48261 | chr1:154399318-154401864 | Psoas_Muscle | SE_48934 | chr1:154399344-154402194 | Right_Atrium | SE_50453 | chr1:154399516-154401315 | Sigmoid_Colon | SE_51380 | chr1:154399138-154401914 | Skeletal_Muscle | SE_52880 | chr1:154399518-154401631 | Small_Intestine | SE_54618 | chr1:154399097-154409137 | Stomach_Smooth_Muscle | SE_62668 | chr1:154357227-154415486 | Tonsil | SE_65390 | chr1:154399323-154400849 | Pancreatic_islets | SE_65390 | chr1:154400868-154402476 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 154399696 | 154400530 | chr1 | 154399716 | 154400696 | chr1 | 154400830 | 154400990 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I154427 | chr1 | 154399576 | 154401508 |
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Enhancer Sequence | ACAAAAAAAG GAAAAAATTA GCCGGGCATG GTGGTGTGTG CCTGTAGTCC CAACTACTCG 60 GGAGGCTGAG ACAGGAGAAT TGCTTGAACC CAGGAGGTTG AGGATGCAGT GAGCCGAGAT 120 CGCGCCATTG CACTCCAGCC TGGGTGATAG AGCGAGATTC TGTCTCAAAA AAAAAAAAAA 180 AGAAAGAAAA GAGAAAAGCA TATCACAGCA GAAGACTATA TTCAAACCAT TTATATGAAG 240 CTCAAAAATG AAGCAAAGTT AAGAAAAATG TAGGGATGTA TGGGTAGTGA AAGTTAGGTT 300 GGTGGGCTTT CCTGGGTATT TTATGCTTCA TAAATTAACT TTTATGTATG TAGCTTTTAC 360 ATACATTATA TATATGAATT TGCATGTATT CAGTATTATG TAATACATTA AAAACAATGT 420 TCGCAATGCT AAAAATATAT TGTTGAAGAT TCTGTGTGAA AGCTATACTG TAGTTGTGGC 480 TTTTTATAAC CCTTTCAAGC CCTCTGGGCA GTAGCAGTCC ACCCCTTATT GCCCTCAGTG 540 GACTTCACCT TCTAGGGACT CAGAATTTTT TTTTTTTTTT TGAGACGGAG CTTCGCTCTT 600 TTTGCCCAGG CTGGAGTGCA GTGGCGTGAT CTCGGCTCAC TGCAAGCTCC GCCTCCCTGG 660 TTCAAGCAAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ATTACAGGAG CCTGCCACCA 720 CGCCCAGCAA ATTTTTTGTA TTTTTAGTAG AGACAGGGTT TCACCATGTT GGCCAGGATG 780 GTCTCGATCT CTTGACTTGT GATCCGTCTC GCCTCGGCCT CCCAAAGTGC TGGGATTACA 840 GGTGTGAGGC CCAGCTGGGA CTCAGATTTT GCTGAGGACC AGGACAGTAC TGTGTGCTGT 900 GTCCTGGCCT TGCAGCAGTG AATGTGTCTC CCGTTTCTCA AGGGCAGGTC TCTGGGATGC 960 CTGACTGTGT CTTCCTTGCC AGTGCCTGGC TGCTGCAGCC TCCTCAAATG TTTATCAAAC 1020 ACAGGACTTG CCCACCGTGG GAGAAAGTAA GGCCATAGGT GTCTCAGGAA CCTGCCCAAA 1080 CTCGCCTGGC TGCACGGTGA CAATTCAACC AGCTTTCTTA CCCAAGGTCT GTTGGTGACC 1140 AGAGAAAACC TTAGATGACC GGCTGCCATG ATGGCCTTAT ATCTGTCCCT TTTCTGCCAG 1200 CCTTGAGGTA GAGGGTGCCA GGGAGGAGGA CTCTGGCTCT AGGTGTTAAA GTGAGAGGGA 1260 AGTGTGAAGG GTATCTGTAT AGCTAGACAG GGCTCAATGC CAGGCAGAGC TGTCTCCGCC 1320 CCTTTGATGT CTATGTCTCT GTCCCTGGAC TGTGGCCAGT AGCCAGTGTG GACTCCAACC 1380 TCACCAGCTT TAGGGGTGTT ATCTGCCTGG GAGTCACTGA TCCTTACTCC CTCCTCTGAC 1440 AGCCACCTTG GATGGGGTGA AAGGAAGGAC AGCCTGCCAA GTATGAGATA AAAACGCCTC 1500 ATAAACAAGA AGGGATTTGC AGGCCAGGCA GAGAGCCTTG TGCTGCTTCT GAGTCCCAGG 1560 AGCATGGGCG AGGAGGTGAG GTCAGGCACT CAGCAGCTGC TGGTCCTCTC TGAAATCTTT 1620 GGCCAGATTT ATTGCTACTG CTTGCTAATA AATGGTTATG CATTTGGTTC AAAGGACCAA 1680 GTGTGCTTAC ATGAAAACTG GCTGTGTTCC CTGGCCTCTG TTTCCTTAGC TGGTTGGACT 1740 AATTTGATTG GTTAATAAAT GAGTCCAAGG TGGTTGGGCT AATTTTTATC TTAGATTCTA 1800 TGACTCTATA ACTGCTACTC AAAAAAAGTG TACTTGTTCC TTTAATCTTT AATCTTATTT 1860 TTCTTGAGTA GTAGAATACA CCCAATTTTT TTCAAGGGGT AGAGAATGCA TTTTTTTTTT 1920 AACCTTCCAG TTTGGTCCCT AGAGTAAACA CAGCATTGCT GTAGTAGATG TAGGGTACTG 1980 GAGGGAGCAT GGAACAGGGA ACCAGAAGCC CTGGTTCCTA CCCCAGCTGG GCATCTGGGC 2040 CAGTCTCTTG ATTCCTCTGT GCCTCAGTTA CCAACTATAT AACGGGCATT CTGCCATGAA 2100 TACCCTGCGA TTTGGAAACC TCCTGTGTAC GTGTGCACTT GGGTGCCTGG CATTCATTCC 2160 TAATGGCATC CATTCGTTCA CACATTCATC CAGTACTCAG CAGACTCCTG CCATGGGCCA 2220 GGCAACGTCC CGGGCACTTG GAATATAATG GAGAACAAAG CAGGGTGCCT ACTTCTGTGG 2280 TGCTTGGAGT CTTGAGGGGA AGAGAGACAC GGAATTCGTA ATTACATGGC AGCGTGTGGG 2340 TGACGTATTG CAGAATGAGG GCCTAGTGGA GCTGGGGGAC CGGAAACGAT GTTTAGGCCG 2400 AGACCTGGAA TAGGAGGAGT TGTCGTGGGG ATGATGTAGG AAGAACGAGT GTGAGGAGGA 2460 GAGCGAGGGG AGTTGAGGGG AGGGCTCCAC ACCTTCTAAG GAGTGGGGAG AGATGAGGCC 2520 TCCAAGGACA GAAGGGCCCT GCAGGCCACG CTGAGGAGCT TGGACTTCAT CTTGTGGATG 2580 GTGGCAGGCC CTTGAAGGGT TTTCTAATCC AGGGAGTGGG GTGGCTGGAT CATGGCTTCA 2640 GAAGGCTCTC CCAGGCAGCT GGATGGTGAA GACCAGGTTG GGGAGGTCAC CAGGAGAATG 2700 CTGCCCTAAT CCAGGCAGAG GTGACGGTAG CCTGGGCCAC TTCATCATTA TCACTGAGGC 2760 CTCTCGTGGC TTCCTCAGAC CAGAACGAAG CCCCCTTCTT CAGTGGCTGT GGGCTCACCA 2820 AGTGTCTTCT CCCTCCTCCA 2840
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