| Tag | Content |
|---|
EnhancerAtlas ID | HS059-26055 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr2:106391950-106394610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr2:106392150-106392162 | GTTTGTTTGTTT | + | 6.32 | | Gata4 | MA0482.1 | chr2:106391989-106392000 | TCTTATCTCCT | + | 6.14 | | NKX2-3 | MA0672.1 | chr2:106394211-106394221 | ACCACTTGAA | + | 6.02 | | SOX10 | MA0442.2 | chr2:106392378-106392389 | AAAACAAAGCA | + | 6.02 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_10292 | chr2:106389778-106395534 | CD19_Primary | | SE_10910 | chr2:106379803-106410786 | CD20 | | SE_11843 | chr2:106390664-106395447 | CD3 | | SE_13211 | chr2:106391758-106392653 | CD34_Primary_RO01480 | | SE_13211 | chr2:106392849-106393497 | CD34_Primary_RO01480 | | SE_14420 | chr2:106390303-106395597 | CD4_Memory_Primary_7pool | | SE_15409 | chr2:106391743-106394581 | CD4_Memory_Primary_8pool | | SE_16297 | chr2:106391802-106395330 | CD4_Naive_Primary_8pool | | SE_17245 | chr2:106391889-106395185 | CD4p_CD225int_CD127p_Tmem | | SE_17337 | chr2:106387664-106410837 | CD4p_CD25-_CD45RAp_Naive | | SE_17777 | chr2:106375854-106401428 | CD4p_CD25-_CD45ROp_Memory | | SE_18243 | chr2:106389599-106421920 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19126 | chr2:106390435-106395412 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20619 | chr2:106390549-106395195 | CD56 | | SE_21274 | chr2:106391998-106395105 | CD8_Memory_7pool | | SE_21873 | chr2:106392019-106395392 | CD8_Naive_7pool | | SE_21946 | chr2:106391596-106395386 | CD8_Naive_8pool | | SE_22311 | chr2:106387922-106395567 | CD8_primiary | | SE_37706 | chr2:106392468-106395199 | HSMMtube | | SE_39779 | chr2:106391878-106392519 | Jurkat | | SE_39779 | chr2:106392544-106393929 | Jurkat | | SE_53622 | chr2:106392083-106394914 | Spleen | | SE_62262 | chr2:106353762-106421483 | Tonsil | | SE_66643 | chr2:106391878-106392519 | Jurkat | | SE_66643 | chr2:106392544-106393929 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I105771 | chr2 | 106387676 | 106396313 |
|
Enhancer Sequence | TTTTTTTCAG TTGTCATTGT AGCACATTGA TGTGTTCTTT CTTATCTCCT TTTGGGTTTT 60
AAACATTATT TATGAATTTA TGCCTTAACT TAAATTGTCT ACAGCTTCTG CTGTAGACAA 120
AGGAGCTGTT TGTTTCATGC AACCTTTCAA GTGAAGAATA ATCAGCTAAT TACAACTGTT 180
TGAAAATTAG CTTCCTTTTT GTTTGTTTGT TTTTCCTTCC TACCCTGGGA GCCTGGCTGG 240
CATCACTGGG AGCACCACAC CTCCCGGTGT GGTGAGCTTG GGAGCTACCT TGATTCACTT 300
GGATTCTTTT AATGTGTATT TGTGTTTTTG TGCACTAATC AGGCTCATTA TTTTCTCATC 360
TGTAAATGAG AAACTTGGAA TAGCTGGTCA TCAAAAAGTT CCTTTTTGAT TTTGTGGTTA 420
CCAAAACCAA AACAAAGCAC CACCACCAAC AAAAAAAACA GTGCGAGGGA TAATTGTTGA 480
CCGTCAGTTG CTTAGGGAGT TAATGACTTC CACCTGGGAA ATAATTTGAA AAAATGTCCC 540
CCTTGTATTT TGGTTTGGCC CAATTTGGTG TGGCCTGGAG CATGTCCCTT ACTGCAGGCC 600
ACCTCTGGGG GTGTGGGTGC GGAGCAGGCC ATGCCTGGCT GGGGACCTCC CCTAGGAATC 660
TCAGTGCTCT GCCCTGCCAT TCGCTCCCAC TTCCTGTACG TTGCTACAGT GTCCTGGGTG 720
GGGACACCCC AACTTCCGTC CCAGCGACAG AAACCGTACA TCCTGGGTTT TCTGTAACAC 780
TCAGTTTCTT ACCTTTTGCC CTTTATTTCT ATAAGTCCTC CAAATATCTT AACATTTCAA 840
CATCTTCTGG AAGCAGCCAA AGCACGTTTG GGGGAGGGAG TTCAGAACCC CTGTCACCAT 900
GCATATACCA GGTGGGCCCA TTTGACTGGG ACAGGGTGGC CGCCCTCCAG GGTGTACAGT 960
CACCCAGCTG TGGTTGGGGG CTGCTTCCTG TGCCATGCCA TCTGCTAGCC TACCCACCCG 1020
TGGAGGGCTC CTGCATGCTG CCAGCCTTGG GTTGTCCCCT GGCCTGGCAG GGGACCTCTA 1080
TGACATTTTG AGCATGATCA GAAAAAGGAA CTTGTGGATT TTCTTTTAGG GTTAGCTGGT 1140
GAGCAGATGA TGCCAGCTAG CAAGCCACCT TCCTCCTCCA GCCAGCCTCC CTCGTTTTAG 1200
CTCAGCCATC CCAGCAGGGC TGGACTTAGT CCAGGCTCCG GGCTCCCAGC TCCTGGCTGC 1260
AGGGATCTTT AGCAGTCGGA CCACACGTGA CTATTCGAGG GTACCATAGC CCTCTGGTTT 1320
CTTTCTGGTA GTCAGTACTG CTGACCTCAC TTTTCAGATA ATCTCTGCTC TCCTCTGGCC 1380
TTGGGGTTCT TCCTGACCCC TTGGAGCCTC TCTCAGTAAA TGGAAACCTC CTAGGGGTTT 1440
CATATAGGCA GAATCTAGTA TGGGGAGTGG CTTCACGAGA GTGTGAAGGG CTGGACAGCC 1500
AAAGGCATCT TCCCCAGAGA TCAGAGACTA AGAAAGCTGC CGCTGTCCCT AGGTCTGAAG 1560
GGCAAAATGA GGCCTTGAGA GTTCCCAGAG CCTGAGAGCA GGTGCTCTCC TCACTGCTGC 1620
TGCCGCCGAG CAGGAATTCT GAGCCCACGG CCCTGCGGCT GTCACTGGGC ACTCCACCGA 1680
TGGCAGCTGG AACCTTCTAC TCTCGTCACT GCTGCTTTAG GAACCTGCTG TCCCCATAGC 1740
CACGAGCCGG GGTGTTGCGG GGGGGCAACG CTTTGCCCTT CCTCCTGCCT TTTAATGTTG 1800
CACCTGGTTG TGTCTTTGAC AGAACTTAAC CAGAATCCAG CTGGCAAGGG TAGCTTTCAG 1860
GTACAGAGGA GGGCTGGGGC AGTCCTCACA CCAGGAGGCC ACATCTTGCA CACAGACTCC 1920
TGAGAGTGTG GGTGGAATGA AATGACCCAG TGCTCACCAC CTGGCACGGC GTGGGTGGAG 1980
AGTGGTAGGT GCTGTGCATT TTCTGTATGG ATCAATGGAA ATGGGATATT GATAATCATG 2040
CGGATTATAC CCACACACCA AAATGGAAAA ACAAAACAAA TGAAAAGTTT AACATGACCT 2100
GCTTTGGCCA GTGGAAATGA CTATAAATGA CTTCAGTTGC AGCTGTTCTC CGGGTAACAG 2160
TCTGTGGACA CCAATGCGCA CAATTCCTAT CAAGGTCCTG TGTGTAGAGC CACTGTGGAC 2220
ACTGTGGTTC TCTGGTGCAT ATGTTGTGGG TGGAGAAGCA GACCACTTGA AGCCCTGGTA 2280
GGAACTGTTT GCTCCTGTCA AGCAGGAAAC AAACACGTGC ATCTTGAAAA TGCCGAGCTC 2340
CCTTTGCAGT TCTGTGCTCG TATTGAAGAG AGGATCGGTA CTGGGGTGAC AGCTCACAGG 2400
ATTCCAGCAG CAGCACCTTG GTTTCGCCTA GCCGTTCAGC CTTTGCCTGT CTTCTTGTCA 2460
TGGAAAGTTC TTTTGTTTGA GACCTGGACT TTGTGAGTCT CTCCTAGCTC CCTTATTTGC 2520
ACCTGCCTTT TCTCCTCACC TTCTTCAGCT GTGCTTGGAG GAGCTGCCAA AGTGGCAGTA 2580
AAAGAAACCC CATTGAGCTC TGTGAAGTGA GAGAAATTTG TCCTAAGGAC AAGATGTGTT 2640
GTGAAGGAGA TGTTGGCAGG 2660
|
