| Tag | Content |
|---|
EnhancerAtlas ID | HS047-18815 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:42332330-42335100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr2:42332676-42332686 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr2:42332676-42332686 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr2:42332676-42332686 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr2:42332676-42332686 | AACAGCTGTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
| SE_10312 | chr2:42325221-42336343 | CD19_Primary | | SE_11146 | chr2:42323572-42336874 | CD20 | | SE_11946 | chr2:42327841-42337002 | CD3 | | SE_14693 | chr2:42327772-42338606 | CD4_Memory_Primary_7pool | | SE_16102 | chr2:42330639-42336500 | CD4_Naive_Primary_7pool | | SE_16740 | chr2:42330928-42334630 | CD4_Naive_Primary_8pool | | SE_16987 | chr2:42327433-42336274 | CD4p_CD225int_CD127p_Tmem | | SE_17444 | chr2:42325062-42338640 | CD4p_CD25-_CD45RAp_Naive | | SE_17811 | chr2:42325303-42338643 | CD4p_CD25-_CD45ROp_Memory | | SE_18685 | chr2:42325197-42338156 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19964 | chr2:42327606-42335969 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20190 | chr2:42327806-42336196 | CD56 | | SE_21801 | chr2:42328127-42336332 | CD8_Naive_7pool | | SE_22420 | chr2:42327613-42337810 | CD8_primiary | | SE_30543 | chr2:42332455-42333846 | Fetal_Muscle | | SE_43599 | chr2:42327765-42335085 | MM1S | | SE_50137 | chr2:42330972-42335286 | Sigmoid_Colon | | SE_53105 | chr2:42331604-42335241 | Small_Intestine | | SE_53609 | chr2:42330894-42335238 | Spleen | | SE_55583 | chr2:42331692-42334918 | Thymus | | SE_62313 | chr2:42323195-42370065 | Tonsil | | SE_67366 | chr2:42327765-42335085 | MM1S |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 42332532 | 42332812 | | chr2 | 42333001 | 42333603 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I042097 | chr2 | 42324141 | 42336955 |
|
Enhancer Sequence | TTTGTAAACA GTTTCCCCAA AACTAAAAAT CTGGCCACAC TGACCTGTAT TCTGCAGTCT 60
ACCACAGGCT CCACCATCCC ATCCTGTCTC TTTCTCTCAC CAACTGCTTG GCCCACCCCT 120
CCTCTCACAC CAAAATGCAA ATATTCCCTA AACAGGTAAC TATTGAATCT AACTAGTCAC 180
ATCGCAGCAT GGAGATCTTA TTCTGAGAGC TGGTTAAGGG AAATTAATTG AGGTAAATTA 240
CGGAGAGAAA GCATTGCTCC GCCAGACAGC GTCAGGCCAT GGCCAGAGCA CAGCAGAAAA 300
GATTTCTACA GTTCTATAAA ACCACAAGAC GAGAAGTTGG TGTTTAAACA GCTGTTATGA 360
AACTAGGGTG TGTGACAGAA ACATCACCTG TTTCCCAAGA GCTCATCCTC TCACTTAATT 420
CAGCAAACAC CAAGCTTTTC TTAGCATCCT GGGCCCCCTT CCCTGCAACT CTTCTTTGGC 480
AGTGCCTTGG GTGATAGTCA GAGGCAAAGT CTGGAGGTGA TTAGATGGCT GCCGACTTAG 540
GCTATAAGCG AGTCCAAAGG AATGGATCTG GCTTTTGATC AGGACAAAGC TACGTCCAGA 600
GGAGAAGCTG AGTGAAGAGG AGGCACCAGT GATAAACTTG GGTTTGAGCA GCCAGGATGG 660
AAGCACGATC TCATTCACCA AGATGGTGAG CAGCTGTGTT CTCTGAAACA CAGACCACGT 720
GAGCAAAAAT TGTCTTCCCC CAATTTGGAG GCTCCTCCCG CCAAAGCAGT TTAATGGGCA 780
GGCAGAGAGG AGGCAGAGTG AGGGAAGGTT TTATATGGAA ATGTGGGAAT GAATGAAAAG 840
GCCTTACTTA AAAGGATCTA TCTGATAGCC CTTGGGACAG CCTCAACCAT CCCCAAATGC 900
CTCTCTGGGG GGTGGGGAGG CATTCAGCTC TGTGGATATT TGAACTCCGA CTGTTTTTGA 960
AAGTCGCCCA TGTGACAAAT GTGTCAACAG AGCCCCGGAT GTGCCCTCTG GGGTGGGGAG 1020
GAGGGTGGAT GTGATCAAGT ACATTTCAGG CTTTCAGAGA AACAGGAAAT TCAGTAATCA 1080
GAGAGCAAAA AATCTATTCA ATCTCTTTTA AAGCCAGTGA ATAATGTAGC AGAGTCAGAA 1140
TTGTCACAAC CGCTGGGTGC AGCTTTGGAA AAGATGAAAG ATGAGAGAAT AGGAGAGGAG 1200
GAGGAGAGGC CCCTGCAGCT GGGATCACTC AGAGACACTC TCCTAACCTT CTCCTTCACC 1260
ATCTGGTGGG AAGAAGGAGC CCCTGAAACT TCTCCTCGAC CCCAACACTC ACCGCCTCGC 1320
CACCATCATC TGCCTTGCAT CCAAAGAAGC TCATCTCATC GTGCCTTTGC CCCTATTGAC 1380
ATCGGTCCTA AGAGCTGCTT GGTTCCCAGC TCACCTAATC TCAGCCCACG AATCCCCAGG 1440
AGGCTACGTA TTTTCCCTAT CCCGGGGCTT TCTTCCACCC TCCCCAACTC CTGAAACTCA 1500
TCCTCCATGC CCTCTGGAGT CCACGATCCA TGATTAGCAA AATCTGTTTT ATCCTCAATC 1560
TATTCTCTCA ACATCTGCCT CACTTCTTTC CCTAAGGGGC ACCTGATTGT CCCCTGAGCT 1620
CACTGCTTTT TCCAACACCT TCTCAAGCAG GGGCTATTTT GTTCTCTCAC AGGCTTCTCA 1680
CTGAGAGGTG ACATAGGTGT CCTTCTTACT CCTCATGGTC ACTTTCAGAA ATATCTCCCT 1740
CCTCCTCTGC AAACCCTTGC ACCCCACATT GAATTTTATA TCTTCAGATT ACATAAATCA 1800
CTACTGTCTT ATCCTGATGC CCAGAGGTCA TTTTTCAATT ATTTTAGGGC CTGGCTAACT 1860
GTTTCTCTAA TATGTACTGT CTTAATGCTT GGTGATTACA ATGTACGCGT AGATAACCCT 1920
TTCAACACCT GAGCCTCTCA GTGCCTTGAA CTTCTTTCCT CCAATGATCT TTCCTCTACT 1980
CAACCCATAA TTGTGATTAC TTACAACTGC AACCTCTCCA TAATCTCAGT TTCATGCATT 2040
CCACTCTCTG ACTGCAACCT CCTATCTTTC CAGTTCATCT CACACATCCC AGCCATCCTT 2100
TGACCCCATC CGAGCCATAC ACTGTTGCCT ACCCTGTGAT GTTCCTACTC CCCTACTGAC 2160
CGTGTCAATT TCATGGTTCA GCCGTTATCA TCATTGCCCC TTCTGTACAC CTTCAGCTCT 2220
TTGCTTCTCT TTTCCTTTGT CACATTCACC TAGCCTGAGG CAGACTTAGT CAAATCCAAC 2280
TCTGCACCTA CTTCATACCT CCACATCTGC TGCTGAACAT GGCTGGAGAA CAACACACAG 2340
CCACACTGCT TGATTCACTT TAAATTCATG ATGATGAAAC TCCATGGGCC CTTAATGCTG 2400
ATCAGGTCAT CTTCCCTGAT GCATTCATTC ACTTTTCCTC CTAGACAGCA GTTTCATACC 2460
TTCTTTTCTC TTCTCAAACC CTTAGCATTT CCTTCCCACC CTTACTTTCA GCTGATAATT 2520
GTATTCTTTC TCCACTGGGA AAATAGAAGC AACCAGGAAA GAACTCTACA GATTCCCACT 2580
ACCACATTTA TCCCCTGACC AGAAGTTGCA TCTTCACACT TTCCACCTAT TACCTGCCCA 2640
TCAAAGCACA TTCCTCGACT TGTGCACACA ATCCTGCCCC TTTCACCTAC TCAAGGACAT 2700
TACTCCAGCA ATGCTTCCCT TTCTCTCTTC CACCAAATTC TCTCTCTCTC TGTCTCTGTC 2760
TCTACTGGAT 2770
|
