Tag | Content |
---|
EnhancerAtlas ID | HS149-01085 |
Organism | Homo sapiens |
Tissue/cell | NKC |
Coordinate | chr7:104595820-104598440 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:104597134-104597149 | TGAACTTCTGACCTC | - | 6.38 | RARA | MA0729.1 | chr7:104597131-104597149 | TCTTGAACTTCTGACCTC | - | 6.88 | ZNF263 | MA0528.1 | chr7:104595858-104595879 | CATTCTTCACCCTTCTCCTCC | - | 6.01 | ZNF263 | MA0528.1 | chr7:104595861-104595882 | TCTTCACCCTTCTCCTCCCTT | - | 6.18 | ZNF263 | MA0528.1 | chr7:104595867-104595888 | CCCTTCTCCTCCCTTTCCTCT | - | 6.31 |
|
| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_02797 | chr7:104597100-104598363 | Astrocytes | SE_09206 | chr7:104596230-104599708 | CD14 | SE_10864 | chr7:104596230-104598721 | CD20 | SE_12036 | chr7:104597035-104598349 | CD3 | SE_14944 | chr7:104597249-104598332 | CD4_Memory_Primary_7pool | SE_16497 | chr7:104597305-104598065 | CD4_Naive_Primary_8pool | SE_19949 | chr7:104596740-104598426 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20140 | chr7:104596124-104598566 | CD56 | SE_21621 | chr7:104597338-104598449 | CD8_Naive_7pool | SE_22586 | chr7:104596522-104598442 | CD8_primiary | SE_23243 | chr7:104597658-104598432 | Colon_Crypt_1 | SE_23896 | chr7:104597720-104598271 | Colon_Crypt_2 | SE_25883 | chr7:104596585-104598467 | Duodenum_Smooth_Muscle | SE_27138 | chr7:104597660-104598437 | Esophagus | SE_31758 | chr7:104597598-104598480 | Gastric | SE_36016 | chr7:104596796-104598440 | HMEC | SE_40784 | chr7:104597781-104598432 | Left_Ventricle | SE_42639 | chr7:104597540-104598428 | Lung | SE_43684 | chr7:104595519-104598465 | MM1S | SE_44335 | chr7:104596231-104599334 | NHDF-Ad | SE_44865 | chr7:104596555-104599531 | NHLF | SE_45643 | chr7:104596366-104599440 | Osteoblasts | SE_50161 | chr7:104596733-104598540 | Sigmoid_Colon | SE_52521 | chr7:104596755-104598388 | Small_Intestine | SE_54878 | chr7:104596388-104599804 | Stomach_Smooth_Muscle | SE_56051 | chr7:104596301-104598585 | u87 | SE_67251 | chr7:104595519-104598465 | MM1S |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 2 | ID | Chromosome | Start | End |
GH07I104955 | chr7 | 104595500 | 104595824 | GH07I104956 | chr7 | 104596512 | 104599449 |
|
Enhancer Sequence | CTTCCAAGCA GTGGCTTGGA ACAAGCCACT CTCAGGGACA TTCTTCACCC TTCTCCTCCC 60 TTTCCTCTCA CTTCAGTCAT TGCTGTTACA TAAACTCTGT CATCATTCTT TCCCCTGAAG 120 TTCAAGTTTG CTTATCTGGG CAGTACCTTT TTCCAATGGG CTGGCCTGTA GTGAGCTTTG 180 TCAGACATGC AGGTCTTCAT ATACTAACCA AAGGATCCTT CAGTTCTTAT GTTACCTTTT 240 TTTTTTTTTT TTTTTTTTTT TTTTGAGACA GGGTGTTGCT CTGTTGCCCT GGCTGGAGTG 300 CAGTGGTGTG ATCATGGCTC ACTGCAGCCT TGATTTCCTG GGCTCAGGTG ATTCTCCCAC 360 CTCATTCTCC TGAGTAGCTG GGATTACAGG TGAACACCAC CATGCCCAGC TAATTTTTTT 420 TTTTCTTTTG GCATTTTTGT ATTTTGGGTA GAAATGGGTT TTCACCATGT TTCCCTGTCA 480 CTCCAGGACT CAAGTGATCT CTCCACCTCA GCCTCCCAAA ATGCAGGGAT TACAGGCATG 540 AGCCACCGTG CCTGGCCCTG TTACATTTCT TTTAACATTT TATAATTCTC AAACTTTGAG 600 AAAGCAAAAC CATAACCTAG CATCCAAAGA AAGGCAATTT GAAAGCTGGC TGATTAGCTT 660 TTTGTTTTAA ATAGCTAGCT TGTCTTGCCA TTTCAAGGCA CTTAGTTTAA TTTTTGGCCC 720 TTTCTTGCTT ATAATTTACC AAGTGCACAA TATTGTAGGT TAGCAAGATT TGGACTCTTT 780 GCCCTTGGTT CAGGCTCTGA TGTTGTGATT CCCCTAAAGT GCATGTTTGA TTTTACACAC 840 TCTACACCCT TCTCTTACTC AATCAAGATA TGGAAATAAA TAAAAATGTC TATTTCATAC 900 TTACCATATC TCCCTTTGGA AGAAAATTGC AAGGCGTAAG AGAATTCCCT AAGAAACGTA 960 CCTTAAAAGA TAAAACTGGA CTCCAGAAAA TTTGCCAGAC TGGGTTGCCA GACTGAACTG 1020 TTCAACAGCC TCTCTGTGTG ATTCCAAATG CCTTGGCCAC CAAACTCCTC TTAGGACCTC 1080 CTTTGATTGT AAGTCAAATT TACACGCAAC CAGTATTTCT TTGTCACTGC TTAGCTGCTT 1140 TTCTGCTTAT TCCATTAAGA TGAGCAATGT GACCAGCTAT CCTTGGGAAG TGAATGCTTG 1200 CTTGGTTTGG TTATCTTGCT ATCATGACAA AATCTAAACT TATTTCACCT TTATAAAAAT 1260 CAGTCAGGAC TATGTATTTT GGGGGCGGTC TTGCTATGTT GCTCAGGCTG GTCTTGAACT 1320 TCTGACCTCA AGTGATCCTC CCACCTTGGT ATCTCAAAGT GTTGAGATTA CAGGTGTGAG 1380 CCACTATGGC CACCCAGAAT CATGTGTTGT ATGATTCCAC TTATATAAAA TATCCAGAAT 1440 AGGTAAATCC ACAGAGACAG AAAGCAGATT AGTGGTTGGC TAGGGCCTGG GGTGTTTGGG 1500 CAGAAATAGG AACGACAGCT TTTGGGGATG AGGTTTCTTT TGGGGGTGAT TAAAATGTTC 1560 TGAAGTTGTT TGTGCTGATG GTTGCACAAT TTTGTGAAAC CAAATGGTAA AAACCATTGA 1620 ATTGTGCATT TTAAATGGAT GAATTGTATG GAACATGAAT TGTATCTCAA TAAAGCTGTT 1680 ATTTAAAAGA AAAAAGTCAG GAATTACTCA GGCGACACTG AAGAGGATGT GTACATGGCT 1740 TCTTTCCATG GAAGGAGACA AACCACCTTG TATTATTGAA GAGAAAGACT CTGGTATCCC 1800 AGCCTTCTAC TCTTACTATA TACACAGTTT CTATTTTGGT CCTTTTTAAA GCCTTCTTGT 1860 TATAGTTAGT GAGCAACAGT TAAGTCGAAA ACCACAGTGA GGCCTTGGTT ACAGCTTACC 1920 CTTGTTTTCA ATCAACAAAA AATATGACTA ATGTCACTGT GGCTCGACTC AACCACATAT 1980 GTGGATTCAG GAGGCTTTGG ACATGTGCTA GAGGCTGCTG GGGCTGACCA GCTGGAAGGA 2040 CAGCAGTTAG CTGAACTTAG GCTCCAGGAA TAAGATGTTG GTGAAGCCTG GGAAAATGTC 2100 TTCCGTGAGC TGGGGGTGGA AAGTTGTTGT GGAAGTAACC CTGAAGGAAA AAAGAGTTCT 2160 CTGGCTGGCT TGGCCCAGAG ATACAGGCTG GAAATTAGTA AGAAGAGCAG ATTTTGAGGC 2220 CAGCATTTCT CTAGCTAACT TCTAGCCCAG CGCCCCTTTT CCATCCTACT ATTTCATACA 2280 TGACCCCCAA GGGAAGCCAT ATCAGGTTCC TAGAGTTGGG AGAAGAGAGA CTCAGGGGGA 2340 ACCTGTACTG AAGTGACTGT GGCAGAGGCA GGGTGAGGCT GAAGAGCACC AGAACATGAG 2400 ACATTTCCCC GCTGTCACTT AGTAACAAGG GCCCTGTGAT GATTAATTTT ATCTGTCAAC 2460 TTGAGGGAGG CTGAGGCACA AGAATTGCTT GAGCCTGGGA GGTAGAAGTT GCAGTGAGCC 2520 AAGATCGTGC CACTGCACTC CAGCCTGGGC AACAAAGTGA GACTCCATCT CAAAAAATAA 2580 AATAAAAATA CAATACAATA CAATAAAATT GGCCGGGCAC 2620
|