Tag | Content |
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EnhancerAtlas ID | HS176-12517 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr14:55574080-55575450 |
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 | TTTTTAGTAG AGATAGGGTT TCACCATGTT GGCCAGGCTG GTCTTGAACT GCCTACCTCA 60 GGTGATCCAC CCACCTTGGC CTCCCAAAGT GCTGGGATTA CAGGCGTAAG CCACCTGCGC 120 CTGGCCGGTA TTTTTAAATT AGAGTTCTTC TAAGATTTAT CTGAAAAAGT TACACTACTA 180 AAAAATTTGC AACCCACACC CAAGGACATA ATTTGTCTGG GCATAGAGAC TTGATGGCAC 240 TTCAAGTAGC TGGATGAGCT TCTCTTAACA TGCGATTTCT CTCAGGTTTA CATTCTTCTT 300 GACTGCCCTT GTTCCTTTCC TATTCTATTT GAAGCAAAAT GGTTAACGTT CTTCCACTTT 360 CACCAGGACA GCCCTATTTG CCCCTTCCTT GTCCTTGTTA GCCTGGTTTT ATAAAGCCTC 420 TTTTGCAGGG GTCGGAACAG TTAATAGCAT TGGGGATTGT CGCTTGTTCC CTGTAGATGA 480 AAAGTATTTT TCTATTGTTT AAAAAAAAAT CGAGGTCATT CTCCAAAGTA ATTTCCTGAA 540 ATAAAGCGTG GGAGGAAGTC ATGGGCATGA GGATGAGTCA TCAGGCAGCA GCACGAGGCT 600 GCAGGCGTGA GCTGGGGAGC CCTGGCTCAG TCCTCCGCAG GCTTGGATCC CTGAGCGGAG 660 CAGGCCACTG GGGCCTTCTG CCGTGAGAAG AGACCTACTG AGAGGCGGGG AGTGGGGGTG 720 GGAGTGGTTG CTTCTGACCT GTAGGACAGT GGTCAGCGTG GGCGGGTGGA GGCACAGGAG 780 AAGGCCGACA GGCCCTGGGT CCTAGGGCCA CTCAGCTGCT GGAAAATGAA GTTCAGAGTT 840 GTTTGGACTG TCTGAAGTAG GATAGAACCA GCCTTAGCCC TAGTTAGGTA ACACATGGCA 900 GAGGCACCTG AGCAAAGACG TGAGCTGGAC CATGGGCTTC CTGGCAGGAC TTCCACGGAG 960 GAGGGCGAGG GGAGAGGAGC AAGGGAGCAG AAGGCAGCTT GCCGTCCACG AAGCCTCCTG 1020 AGGCCCCAGA TGAGTCACCA GACAACAGCC TGTCTACTTA AAGCAACTGC TGGGCAACTG 1080 CTGAGTAGAA CAGTCCCTAA CCACATGAAC ACTGGGGAGG AGGTTCTGAA AGACGCTGCT 1140 GGGTGCAAGG TCCCTAACTA GGGTAATCCA ATTTCACTCC AGGCTAACAT GAGAAATTAT 1200 GACTCCAGCA GCCAATCCTG TGGGCCGTGA GAGAGTGGGA GAGGGATTTT CCAGATATAA 1260 GTCCCACTAG AGCTTCTTTT TTTTTTTTTT TTTTGATACG GAGTCTCACT CTGTTATCCA 1320 CGCTGGAGTG CAGTGGCACC ATCTCGGCTC ACTGCAAGCT CCGCCTCCCG 1370
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