Tag | Content |
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EnhancerAtlas ID | HS048-17987 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr18:74783120-74784580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr18:74783862-74783873 | TTTCCCAGAAG | - | 6.62 | ZNF263 | MA0528.1 | chr18:74784111-74784132 | CCTCCCCTCCCCTCCTGCCTC | - | 6.73 |
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| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_02301 | chr18:74782001-74785139 | Astrocytes | SE_09139 | chr18:74771371-74785241 | CD14 | SE_11015 | chr18:74762704-74785115 | CD20 | SE_12115 | chr18:74778461-74787202 | CD3 | SE_13673 | chr18:74784180-74785205 | CD34_Primary_RO01536 | SE_15038 | chr18:74778576-74784852 | CD4_Memory_Primary_7pool | SE_15651 | chr18:74778509-74786225 | CD4_Memory_Primary_8pool | SE_16468 | chr18:74778596-74785053 | CD4_Naive_Primary_8pool | SE_17255 | chr18:74778864-74784019 | CD4p_CD225int_CD127p_Tmem | SE_17959 | chr18:74771488-74787372 | CD4p_CD25-_CD45ROp_Memory | SE_18700 | chr18:74771421-74787762 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19374 | chr18:74778282-74785130 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19981 | chr18:74771452-74788754 | CD56 | SE_21261 | chr18:74778550-74784923 | CD8_Memory_7pool | SE_22307 | chr18:74770375-74789123 | CD8_primiary | SE_25341 | chr18:74771526-74785162 | DND41 | SE_25885 | chr18:74783911-74785197 | Duodenum_Smooth_Muscle | SE_26884 | chr18:74782489-74784977 | Esophagus | SE_30168 | chr18:74783191-74784494 | Fetal_Muscle | SE_34994 | chr18:74773337-74785172 | HeLa | SE_39197 | chr18:74776594-74786600 | IMR90 | SE_41189 | chr18:74783193-74785058 | Left_Ventricle | SE_42218 | chr18:74783324-74785105 | Lung | SE_44218 | chr18:74782828-74785072 | NHDF-Ad | SE_47137 | chr18:74774037-74784811 | Panc1 | SE_49182 | chr18:74783332-74784361 | Right_Atrium | SE_51089 | chr18:74782985-74785181 | Skeletal_Muscle | SE_52417 | chr18:74782923-74785054 | Small_Intestine | SE_53332 | chr18:74771633-74785069 | Spleen | SE_58547 | chr18:74756065-74865317 | Ly1 | SE_61817 | chr18:74764079-74793826 | Toledo | SE_62620 | chr18:74763866-74793718 | Tonsil | SE_65082 | chr18:74774799-74784762 | NHEK | SE_65574 | chr18:74784130-74784965 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I077059 | chr18 | 74771556 | 74787401 |
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Enhancer Sequence | CATTATACAG CATATTCTTA AAGTCCTGAT TCAGACTAGA AACTGCTTAT CAGGAGAGGA 60 AGGTGTTGAA ACATGTTACA AAGTGACTCT CACCTGCAAA ACCAGTTGTA TGTTAGACTC 120 GGAGTCATGG TCCACCACAG GCTGCTGTAT TCAACACATG TAAGAGTTGA TTTTGAGAAT 180 TTTTCAATCC CTTAAAAAAT GCTGCATTTC CCTTAAAAAA TGCTGCATTA GGAGATGTCC 240 TAAGCTTGTC CAGCCCATCT TATTTTGTTG TTGCTCTTCT GTTTTGTTTT GTTTTAGGCT 300 TTTAGCAACC TGAAGCCATG GTTTTTAGTT TCTGTCTCTA GTGATAACCA GAACAGAAAG 360 ATGAGGAAGG GTCTTTACTG ACCCAACCAG GGACAGAAAC TAAGAATCCA TGACTGTATT 420 CTCTCCTTGG ACACTTGAAG CCTTGAGTGG AGAATCACTG GCCTGGAAGC AGATAAAAGT 480 CTTGTCTGGT TCTGCATCCT CAGTACCTTG CCACTCACCC ACTTGTTCCC ACCCATGCTT 540 GCACCAAACC CTGCTCAGGA GCTGAGCATA CAAAGAAAAT AAGGTAGGAA GCCAAATTGG 600 GTGCTTCAAA AATAAAGCTA GAGAAGCAAG CCCAGAATGT CAGATGGCGA CTGTCCAATT 660 AAACTCGGTG AGCCAAGCCC TGTCCATCAC ACTGGAGAGT GTCAATGGCG TAGGAAGTGC 720 ACCGTGTTTA TTTTTTCTGA GATTTCCCAG AAGAAAAATT ACAGTGATTC ATATTTCTAA 780 AATTCCTAGG ATGTTTAACA AGAGAAGTTG CAACTGTCTT CCCCCTTCTG AATCTTATAC 840 TCGACTGACC TTATTTAAAA AACAAAACAA ACAAAAAAGC CCAGCTGAAG CTTCCTATGA 900 CGTCACAGGC GACACAGTCA TATGTGGCAC CTACATGCCA GCTGCTTGGC CTTTGAAGGC 960 TCAGGATCCT GCCGGCGTAC ACACCCCTCC GCCTCCCCTC CCCTCCTGCC TCATAATTCT 1020 TATCTCATTT CTATGCACAA ATCTGAATAT GGCCTGGTGT TTCTCACAGC ACCACACATA 1080 TTTTGAGCCT TAGGTCATTT CAGAGGGGAT GCTACTAAAA GGCAGATATT TCTTTAAGTT 1140 TTCTTTACCT TCTGCCATAT TCCCTGCCGT AGACAGATCT AATTCACCCA GATATTTGCA 1200 GAAAATAGTT TGGGGGCATC AGGATCTGCA ACACATGTAC GTCGTATCAA AATCATTATT 1260 CGCATGACAG CCAAGACCTC GGGCTCTCTG AAGCTGATTG CCTGGGTAAC AGGGAAAATA 1320 ACTGAGTTTT CTGTACCTGT TTGCTCAGCT TTAAAATGAA CATTATAATC ATACTTTTCT 1380 ATGTGGTCAT CGTGAAGAGC ATTCAATAAG TGGAAACTGC TCTTTGCAGA AGCACACAAA 1440 ACTATTGAAA ATGCAGATCA 1460
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