Tag | Content |
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EnhancerAtlas ID | HS187-06743 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr13:41591160-41592650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr13:41591718-41591739 | ACCCCCCCTTCTCCCTTCTCC | - | 6.55 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_09221 | chr13:41588268-41594981 | CD14 | SE_10387 | chr13:41591054-41594336 | CD19_Primary | SE_10999 | chr13:41586782-41594964 | CD20 | SE_12017 | chr13:41591113-41594408 | CD3 | SE_12860 | chr13:41591107-41594210 | CD34_Primary_RO01480 | SE_13324 | chr13:41591123-41594688 | CD34_Primary_RO01536 | SE_14054 | chr13:41591043-41594008 | CD34_Primary_RO01549 | SE_14557 | chr13:41591019-41594655 | CD4_Memory_Primary_7pool | SE_17089 | chr13:41591090-41593939 | CD4p_CD225int_CD127p_Tmem | SE_17551 | chr13:41591106-41594888 | CD4p_CD25-_CD45RAp_Naive | SE_18001 | chr13:41587961-41594231 | CD4p_CD25-_CD45ROp_Memory | SE_18357 | chr13:41586465-41594682 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20204 | chr13:41591008-41594260 | CD56 | SE_22365 | chr13:41591055-41594316 | CD8_primiary | SE_25440 | chr13:41591096-41594870 | DND41 | SE_26079 | chr13:41591111-41596208 | Duodenum_Smooth_Muscle | SE_27818 | chr13:41591048-41596772 | Fetal_Intestine | SE_28717 | chr13:41589113-41596566 | Fetal_Intestine_Large | SE_31205 | chr13:41591057-41594339 | Fetal_Thymus | SE_32532 | chr13:41591085-41593864 | GM12878 | SE_35394 | chr13:41591129-41595366 | HepG2 | SE_39455 | chr13:41591106-41593720 | Jurkat | SE_44094 | chr13:41591111-41593840 | MM1S | SE_55509 | chr13:41591230-41591759 | Thymus | SE_58302 | chr13:41534094-41596249 | Ly1 | SE_60466 | chr13:41534866-41594996 | DHL6 | SE_61682 | chr13:41555019-41595174 | Toledo | SE_62237 | chr13:41534318-41594936 | Tonsil | SE_64637 | chr13:41591143-41594546 | NHEK | SE_66291 | chr13:41591106-41593720 | Jurkat |
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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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Enhancer Sequence | AGCTCAAATT TAATTCCCAC CTCTTCATAT TTCCATCTAA AGCCATCTTA AAATAAGCAG 60 TCATGAACAA AAAAATTCTA ACAGTGAAAA ACAAAAAGTT GTTGTAGAAA TAAAATGAAT 120 GCATCATCTT TCTGATGAAA AAGAAAACTA CATTTTCAAA ATCATTGGTT GATCCATTTG 180 GTTGCAACTT ATCACCAAGA TTATCACCAA ACATCTTAAT TAAGGTTTTA TTTACTCTTA 240 AGGAAATATA GAGCATTTCA AACAAAGCAT CACTTGTGAC TGGCACAAGC AGTTCCAGAC 300 TGCGAAGCCC TGCCATTAGG TACTGCATGA CCTCAAGCAA ATCACAGGAC CTCTGTGGGC 360 CACTGTTTCT TCATCTATAA AAGTGAGGCA GTTGGACAAT CTTCAGTCAC TTTCAGCACT 420 AAAGTTCTAT AAATCACTAA TTCTAAATTT AATTCTGATG GGTCAGTTCA AACTTACATT 480 CAATCTTATG GAAGGAAAAA CGTGGAGAGG GAAATACTTA ATAAATTGTT CTGGTCTTTT 540 CTTGGTTCTC TTCTTTTTAC CCCCCCTTCT CCCTTCTCCT TGAAACTCCA CTTCAGTCTC 600 TATCACGTAA GAAAATACAT AAACAATATC TATACTACTT TAACTGTACC AGCTTCTTAA 660 ATTTAAGAAA CCAAATTCCT CTACTTCTCT TTAATAAATA AGATCTTAAT TATGCCGCTT 720 ATTTGTGTGC CTCTTGATTT TTCTCTTATG GATCACCACC TTAAAAAAGT TAAAAAAAAA 780 AATAGAAAAG TCTTCATTAG ATTTTTCACA CAGACCAGAC TAGAAGTAAA TACAGCTTTT 840 GCTTACTCAA AGGCTGACTA AACCAGCAAT ATGCAAACAA AGATGATAGC AAATGGCTCA 900 GCTGAATTGG TAAAATGTCC GCTGTGTCTT TCTTGTAAGA CCGCAAAATT GAGATCTGTT 960 AATATCAACA ATCCTTACAA AAGAGTAAGA AATAATAACT GATTGCCTTT GTCTCTTCCC 1020 TTTAATCTGA CAGGCCTTCA AGCACTTAGT AAGTGCATAG CAAATTCTCA AAGAACTAGC 1080 TAAATATCAT TTTGGTCAAC AAGAAATGAT TTGGCAAGTT TTATATCCAA AAACTTTATT 1140 TTTTGGAATC ACTGCATATT CCAATTTTAT CTTCATAAAT ATGTTTCAGA AATAAAATAC 1200 TACTGCACTC ATCTTTACAG AGCACCTAGA ACTTTAAGGC ACAGTAGGAT GTATACTTGC 1260 CAGCCAAAAT CTCATAACTA CAATGACAAG TACTTCAGGA AAAGACTGAG CAATCTTTTC 1320 ATTTACAGAA GGTTTTTAAT TCAAGGCAGG CAAATTTTAA GAACAGTAAT ACAAAAGGAA 1380 GGCCAATACT CATCACTTTT TCTTTTTACA CAAAATTGAA ATAACTACGT TTCCTTAGAA 1440 GACAGCTTTA CTTCTAAGGT TGTTACTCAG AACAAGTTTT CAGTGTGAAT 1490
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