Tag | Content |
---|
EnhancerAtlas ID | HS179-02177 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr1:154398780-154401670 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| 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 |
|
| 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I154427 | chr1 | 154399576 | 154401508 |
|
Enhancer Sequence | GTTCAAGACC AGCCTGACTA ATATGGTGAA ACCCCATCTC TACTAAAAAT ACAAAAAAAG 60 GAAAAAATTA GCCGGGCATG GTGGTGTGTG CCTGTAGTCC CAACTACTCG GGAGGCTGAG 120 ACAGGAGAAT TGCTTGAACC CAGGAGGTTG AGGATGCAGT GAGCCGAGAT CGCGCCATTG 180 CACTCCAGCC TGGGTGATAG AGCGAGATTC TGTCTCAAAA AAAAAAAAAA AGAAAGAAAA 240 GAGAAAAGCA TATCACAGCA GAAGACTATA TTCAAACCAT TTATATGAAG CTCAAAAATG 300 AAGCAAAGTT AAGAAAAATG TAGGGATGTA TGGGTAGTGA AAGTTAGGTT GGTGGGCTTT 360 CCTGGGTATT TTATGCTTCA TAAATTAACT TTTATGTATG TAGCTTTTAC ATACATTATA 420 TATATGAATT TGCATGTATT CAGTATTATG TAATACATTA AAAACAATGT TCGCAATGCT 480 AAAAATATAT TGTTGAAGAT TCTGTGTGAA AGCTATACTG TAGTTGTGGC TTTTTATAAC 540 CCTTTCAAGC CCTCTGGGCA GTAGCAGTCC ACCCCTTATT GCCCTCAGTG GACTTCACCT 600 TCTAGGGACT CAGAATTTTT TTTTTTTTTT TGAGACGGAG CTTCGCTCTT TTTGCCCAGG 660 CTGGAGTGCA GTGGCGTGAT CTCGGCTCAC TGCAAGCTCC GCCTCCCTGG TTCAAGCAAT 720 TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ATTACAGGAG CCTGCCACCA CGCCCAGCAA 780 ATTTTTTGTA TTTTTAGTAG AGACAGGGTT TCACCATGTT GGCCAGGATG GTCTCGATCT 840 CTTGACTTGT GATCCGTCTC GCCTCGGCCT CCCAAAGTGC TGGGATTACA GGTGTGAGGC 900 CCAGCTGGGA CTCAGATTTT GCTGAGGACC AGGACAGTAC TGTGTGCTGT GTCCTGGCCT 960 TGCAGCAGTG AATGTGTCTC CCGTTTCTCA AGGGCAGGTC TCTGGGATGC CTGACTGTGT 1020 CTTCCTTGCC AGTGCCTGGC TGCTGCAGCC TCCTCAAATG TTTATCAAAC ACAGGACTTG 1080 CCCACCGTGG GAGAAAGTAA GGCCATAGGT GTCTCAGGAA CCTGCCCAAA CTCGCCTGGC 1140 TGCACGGTGA CAATTCAACC AGCTTTCTTA CCCAAGGTCT GTTGGTGACC AGAGAAAACC 1200 TTAGATGACC GGCTGCCATG ATGGCCTTAT ATCTGTCCCT TTTCTGCCAG CCTTGAGGTA 1260 GAGGGTGCCA GGGAGGAGGA CTCTGGCTCT AGGTGTTAAA GTGAGAGGGA AGTGTGAAGG 1320 GTATCTGTAT AGCTAGACAG GGCTCAATGC CAGGCAGAGC TGTCTCCGCC CCTTTGATGT 1380 CTATGTCTCT GTCCCTGGAC TGTGGCCAGT AGCCAGTGTG GACTCCAACC TCACCAGCTT 1440 TAGGGGTGTT ATCTGCCTGG GAGTCACTGA TCCTTACTCC CTCCTCTGAC AGCCACCTTG 1500 GATGGGGTGA AAGGAAGGAC AGCCTGCCAA GTATGAGATA AAAACGCCTC ATAAACAAGA 1560 AGGGATTTGC AGGCCAGGCA GAGAGCCTTG TGCTGCTTCT GAGTCCCAGG AGCATGGGCG 1620 AGGAGGTGAG GTCAGGCACT CAGCAGCTGC TGGTCCTCTC TGAAATCTTT GGCCAGATTT 1680 ATTGCTACTG CTTGCTAATA AATGGTTATG CATTTGGTTC AAAGGACCAA GTGTGCTTAC 1740 ATGAAAACTG GCTGTGTTCC CTGGCCTCTG TTTCCTTAGC TGGTTGGACT AATTTGATTG 1800 GTTAATAAAT GAGTCCAAGG TGGTTGGGCT AATTTTTATC TTAGATTCTA TGACTCTATA 1860 ACTGCTACTC AAAAAAAGTG TACTTGTTCC TTTAATCTTT AATCTTATTT TTCTTGAGTA 1920 GTAGAATACA CCCAATTTTT TTCAAGGGGT AGAGAATGCA TTTTTTTTTT AACCTTCCAG 1980 TTTGGTCCCT AGAGTAAACA CAGCATTGCT GTAGTAGATG TAGGGTACTG GAGGGAGCAT 2040 GGAACAGGGA ACCAGAAGCC CTGGTTCCTA CCCCAGCTGG GCATCTGGGC CAGTCTCTTG 2100 ATTCCTCTGT GCCTCAGTTA CCAACTATAT AACGGGCATT CTGCCATGAA TACCCTGCGA 2160 TTTGGAAACC TCCTGTGTAC GTGTGCACTT GGGTGCCTGG CATTCATTCC TAATGGCATC 2220 CATTCGTTCA CACATTCATC CAGTACTCAG CAGACTCCTG CCATGGGCCA GGCAACGTCC 2280 CGGGCACTTG GAATATAATG GAGAACAAAG CAGGGTGCCT ACTTCTGTGG TGCTTGGAGT 2340 CTTGAGGGGA AGAGAGACAC GGAATTCGTA ATTACATGGC AGCGTGTGGG TGACGTATTG 2400 CAGAATGAGG GCCTAGTGGA GCTGGGGGAC CGGAAACGAT GTTTAGGCCG AGACCTGGAA 2460 TAGGAGGAGT TGTCGTGGGG ATGATGTAGG AAGAACGAGT GTGAGGAGGA GAGCGAGGGG 2520 AGTTGAGGGG AGGGCTCCAC ACCTTCTAAG GAGTGGGGAG AGATGAGGCC TCCAAGGACA 2580 GAAGGGCCCT GCAGGCCACG CTGAGGAGCT TGGACTTCAT CTTGTGGATG GTGGCAGGCC 2640 CTTGAAGGGT TTTCTAATCC AGGGAGTGGG GTGGCTGGAT CATGGCTTCA GAAGGCTCTC 2700 CCAGGCAGCT GGATGGTGAA GACCAGGTTG GGGAGGTCAC CAGGAGAATG CTGCCCTAAT 2760 CCAGGCAGAG GTGACGGTAG CCTGGGCCAC TTCATCATTA TCACTGAGGC CTCTCGTGGC 2820 TTCCTCAGAC CAGAACGAAG CCCCCTTCTT CAGTGGCTGT GGGCTCACCA AGTGTCTTCT 2880 CCCTCCTCCA 2890
|