Tag | Content |
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EnhancerAtlas ID | HS113-11208 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr14:55573550-55575790 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr14:55575108-55575119 | GATGAGTCACC | - | 6.32 | JUND | MA0491.1 | chr14:55575108-55575119 | GATGAGTCACC | - | 6.62 | ZNF263 | MA0528.1 | chr14:55575036-55575057 | GGAGGAGGGCGAGGGGAGAGG | + | 7.74 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00244 | chr14:55563236-55576350 | Adipose_Nuclei | SE_00820 | chr14:55574748-55575102 | Adipose_Tissue | SE_02600 | chr14:55573844-55576160 | Astrocytes | SE_09388 | chr14:55568067-55576360 | CD14 | SE_23110 | chr14:55574129-55575416 | Colon_Crypt_1 | SE_23790 | chr14:55574297-55574562 | Colon_Crypt_2 | SE_23790 | chr14:55574594-55575269 | Colon_Crypt_2 | SE_24786 | chr14:55574109-55575428 | Colon_Crypt_3 | SE_26013 | chr14:55573672-55575878 | Duodenum_Smooth_Muscle | SE_26711 | chr14:55573567-55575917 | Esophagus | SE_27630 | chr14:55573899-55576071 | Fetal_Intestine | SE_28543 | chr14:55573873-55576230 | Fetal_Intestine_Large | SE_31668 | chr14:55574018-55575868 | Gastric | SE_33558 | chr14:55573897-55579764 | H2171 | SE_34039 | chr14:55574107-55575498 | HCC1954 | SE_34802 | chr14:55573592-55576155 | HeLa | SE_36310 | chr14:55573891-55575863 | HMEC | SE_37768 | chr14:55573433-55575974 | HSMMtube | SE_41170 | chr14:55573962-55575665 | Left_Ventricle | SE_42472 | chr14:55573658-55575611 | Lung | SE_44570 | chr14:55573874-55576148 | NHDF-Ad | SE_45117 | chr14:55573558-55575933 | NHLF | SE_46036 | chr14:55573692-55576091 | Osteoblasts | SE_46880 | chr14:55574151-55574573 | Ovary | SE_46880 | chr14:55574627-55575401 | Ovary | SE_49010 | chr14:55574074-55575920 | Right_Atrium | SE_50181 | chr14:55574075-55575919 | Sigmoid_Colon | SE_52430 | chr14:55573656-55575984 | Small_Intestine | SE_56717 | chr14:55573869-55576081 | u87 | SE_57551 | chr14:55574279-55575356 | VACO_503 | SE_64542 | chr14:55574036-55575714 | NHEK | SE_66903 | chr14:55573897-55579764 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 55574264 | 55575347 | chr14 | 55574465 | 55575376 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I055097 | chr14 | 55563775 | 55576469 |
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Enhancer Sequence | AATGAATTTT AACTTAAATG TAGATTCATA AATTATTTCT TTTGTGTTTT TATCTTTTAT 60 TGTTTTTTGA GACAGAGTCT CACTCTGTTG CCCAGGCTGG AGTACAGTGG CTTGATCTCG 120 GCTCACTACA ACCTCCACCT CCTGGTTCAA GTGATTGTCC TGTCTCACCC TCCCCAGTAA 180 CTGGGATTAC AGGCGCCCAC CACCACACCC AGGTAATTCT TGTGTTTTTG TAGAGGTGGG 240 GTCTCGCCAT GTTGTCCAGG CCGGTCTGGA ACTCCTGGCC TCAAGCGATC TGCCCGCCTC 300 AGCCTCCCAA AGTGCTGGGG TTACAGGCGT GAGCCACTGC GCCCGGCCTC CTTGGTATTT 360 TTATGTCTAT TTTTTTAGAT GGAGTCTCGC TCTGTCCCCC AGGCTGGAGT GCAGTGGCGC 420 GATCAGCTCA CTGCAACCTC CACCTCGCGG GTTCAAGCAA TTCTCCTGCC TCAGCCTCCT 480 GAGTAGCTGG GATTACAGAC GTCCATCAAC ACGCCCAGCT AATTTTTGTA TTTTTAGTAG 540 AGATAGGGTT TCACCATGTT GGCCAGGCTG GTCTTGAACT GCCTACCTCA GGTGATCCAC 600 CCACCTTGGC CTCCCAAAGT GCTGGGATTA CAGGCGTAAG CCACCTGCGC CTGGCCGGTA 660 TTTTTAAATT AGAGTTCTTC TAAGATTTAT CTGAAAAAGT TACACTACTA AAAAATTTGC 720 AACCCACACC CAAGGACATA ATTTGTCTGG GCATAGAGAC TTGATGGCAC TTCAAGTAGC 780 TGGATGAGCT TCTCTTAACA TGCGATTTCT CTCAGGTTTA CATTCTTCTT GACTGCCCTT 840 GTTCCTTTCC TATTCTATTT GAAGCAAAAT GGTTAACGTT CTTCCACTTT CACCAGGACA 900 GCCCTATTTG CCCCTTCCTT GTCCTTGTTA GCCTGGTTTT ATAAAGCCTC TTTTGCAGGG 960 GTCGGAACAG TTAATAGCAT TGGGGATTGT CGCTTGTTCC CTGTAGATGA AAAGTATTTT 1020 TCTATTGTTT AAAAAAAAAT CGAGGTCATT CTCCAAAGTA ATTTCCTGAA ATAAAGCGTG 1080 GGAGGAAGTC ATGGGCATGA GGATGAGTCA TCAGGCAGCA GCACGAGGCT GCAGGCGTGA 1140 GCTGGGGAGC CCTGGCTCAG TCCTCCGCAG GCTTGGATCC CTGAGCGGAG CAGGCCACTG 1200 GGGCCTTCTG CCGTGAGAAG AGACCTACTG AGAGGCGGGG AGTGGGGGTG GGAGTGGTTG 1260 CTTCTGACCT GTAGGACAGT GGTCAGCGTG GGCGGGTGGA GGCACAGGAG AAGGCCGACA 1320 GGCCCTGGGT CCTAGGGCCA CTCAGCTGCT GGAAAATGAA GTTCAGAGTT GTTTGGACTG 1380 TCTGAAGTAG GATAGAACCA GCCTTAGCCC TAGTTAGGTA ACACATGGCA GAGGCACCTG 1440 AGCAAAGACG TGAGCTGGAC CATGGGCTTC CTGGCAGGAC TTCCACGGAG GAGGGCGAGG 1500 GGAGAGGAGC AAGGGAGCAG AAGGCAGCTT GCCGTCCACG AAGCCTCCTG AGGCCCCAGA 1560 TGAGTCACCA GACAACAGCC TGTCTACTTA AAGCAACTGC TGGGCAACTG CTGAGTAGAA 1620 CAGTCCCTAA CCACATGAAC ACTGGGGAGG AGGTTCTGAA AGACGCTGCT GGGTGCAAGG 1680 TCCCTAACTA GGGTAATCCA ATTTCACTCC AGGCTAACAT GAGAAATTAT GACTCCAGCA 1740 GCCAATCCTG TGGGCCGTGA GAGAGTGGGA GAGGGATTTT CCAGATATAA GTCCCACTAG 1800 AGCTTCTTTT TTTTTTTTTT TTTTGATACG GAGTCTCACT CTGTTATCCA CGCTGGAGTG 1860 CAGTGGCACC ATCTCGGCTC ACTGCAAGCT CCGCCTCCCG GGTTCAAGCG ATTCTGTTGC 1920 CCCAGCCTCC TGAGCAGATG GGACTACAGA TGTGCACCAC CATGCCCAGC TAATTTTTGT 1980 ATTTTTAGTA GAGACAGGGT TTCACTATGT CGGCCAGGCT GGTCTCGAAC TCCTGACCTC 2040 ATGATTCTCC TGCCTTGGCC TCCTAAAGTG TTGGGATCAC TGGCATAAGC CACAGCTTCC 2100 GGCTGAGTCC CACTAGAGCT TCTAAGAAGA AATTAGGGAA GCAGGATTAT GAGAGGCCTG 2160 GTCCCACTCA CAGTGTGCGA CATCACTGAT GACTATGCTT GGTTACCTGC CTTGTTATTT 2220 GCTACCTTTG TTATTGTCTA 2240
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