Tag | Content |
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EnhancerAtlas ID | HS111-01444 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr14:55574090-55575750 |
Target genes | |
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 | AGATAGGGTT TCACCATGTT GGCCAGGCTG GTCTTGAACT GCCTACCTCA GGTGATCCAC 60 CCACCTTGGC CTCCCAAAGT GCTGGGATTA CAGGCGTAAG CCACCTGCGC CTGGCCGGTA 120 TTTTTAAATT AGAGTTCTTC TAAGATTTAT CTGAAAAAGT TACACTACTA AAAAATTTGC 180 AACCCACACC CAAGGACATA ATTTGTCTGG GCATAGAGAC TTGATGGCAC TTCAAGTAGC 240 TGGATGAGCT TCTCTTAACA TGCGATTTCT CTCAGGTTTA CATTCTTCTT GACTGCCCTT 300 GTTCCTTTCC TATTCTATTT GAAGCAAAAT GGTTAACGTT CTTCCACTTT CACCAGGACA 360 GCCCTATTTG CCCCTTCCTT GTCCTTGTTA GCCTGGTTTT ATAAAGCCTC TTTTGCAGGG 420 GTCGGAACAG TTAATAGCAT TGGGGATTGT CGCTTGTTCC CTGTAGATGA AAAGTATTTT 480 TCTATTGTTT AAAAAAAAAT CGAGGTCATT CTCCAAAGTA ATTTCCTGAA ATAAAGCGTG 540 GGAGGAAGTC ATGGGCATGA GGATGAGTCA TCAGGCAGCA GCACGAGGCT GCAGGCGTGA 600 GCTGGGGAGC CCTGGCTCAG TCCTCCGCAG GCTTGGATCC CTGAGCGGAG CAGGCCACTG 660 GGGCCTTCTG CCGTGAGAAG AGACCTACTG AGAGGCGGGG AGTGGGGGTG GGAGTGGTTG 720 CTTCTGACCT GTAGGACAGT GGTCAGCGTG GGCGGGTGGA GGCACAGGAG AAGGCCGACA 780 GGCCCTGGGT CCTAGGGCCA CTCAGCTGCT GGAAAATGAA GTTCAGAGTT GTTTGGACTG 840 TCTGAAGTAG GATAGAACCA GCCTTAGCCC TAGTTAGGTA ACACATGGCA GAGGCACCTG 900 AGCAAAGACG TGAGCTGGAC CATGGGCTTC CTGGCAGGAC TTCCACGGAG GAGGGCGAGG 960 GGAGAGGAGC AAGGGAGCAG AAGGCAGCTT GCCGTCCACG AAGCCTCCTG AGGCCCCAGA 1020 TGAGTCACCA GACAACAGCC TGTCTACTTA AAGCAACTGC TGGGCAACTG CTGAGTAGAA 1080 CAGTCCCTAA CCACATGAAC ACTGGGGAGG AGGTTCTGAA AGACGCTGCT GGGTGCAAGG 1140 TCCCTAACTA GGGTAATCCA ATTTCACTCC AGGCTAACAT GAGAAATTAT GACTCCAGCA 1200 GCCAATCCTG TGGGCCGTGA GAGAGTGGGA GAGGGATTTT CCAGATATAA GTCCCACTAG 1260 AGCTTCTTTT TTTTTTTTTT TTTTGATACG GAGTCTCACT CTGTTATCCA CGCTGGAGTG 1320 CAGTGGCACC ATCTCGGCTC ACTGCAAGCT CCGCCTCCCG GGTTCAAGCG ATTCTGTTGC 1380 CCCAGCCTCC TGAGCAGATG GGACTACAGA TGTGCACCAC CATGCCCAGC TAATTTTTGT 1440 ATTTTTAGTA GAGACAGGGT TTCACTATGT CGGCCAGGCT GGTCTCGAAC TCCTGACCTC 1500 ATGATTCTCC TGCCTTGGCC TCCTAAAGTG TTGGGATCAC TGGCATAAGC CACAGCTTCC 1560 GGCTGAGTCC CACTAGAGCT TCTAAGAAGA AATTAGGGAA GCAGGATTAT GAGAGGCCTG 1620 GTCCCACTCA CAGTGTGCGA CATCACTGAT GACTATGCTT 1660
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