| Tag | Content |
|---|
EnhancerAtlas ID | HS176-20336 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:43405080-43406610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXF2 | MA0030.1 | chr2:43406393-43406407 | TCAAGGTAAACAAA | + | 6.7 | | ZNF263 | MA0528.1 | chr2:43406196-43406217 | CACCCCTGCTCCCCTTCCTCC | - | 6.38 | | ZNF263 | MA0528.1 | chr2:43405533-43405554 | GGAGGAGGCAGGGCCAGAGGA | + | 6.4 |
|
| | Number of super-enhancer constituents: 45 | ID | Coordinate | Tissue/cell |
| SE_03102 | chr2:43405034-43407173 | Bladder | | SE_09287 | chr2:43404602-43407281 | CD14 | | SE_11722 | chr2:43405238-43406788 | CD20 | | SE_11879 | chr2:43404845-43406867 | CD3 | | SE_12501 | chr2:43405034-43405407 | CD34_adult | | SE_12501 | chr2:43405453-43406127 | CD34_adult | | SE_12501 | chr2:43406426-43406591 | CD34_adult | | SE_12758 | chr2:43405240-43405417 | CD34_fetal | | SE_12758 | chr2:43405497-43405782 | CD34_fetal | | SE_12758 | chr2:43406064-43406264 | CD34_fetal | | SE_13409 | chr2:43404300-43407894 | CD34_Primary_RO01536 | | SE_14384 | chr2:43400219-43408412 | CD4_Memory_Primary_7pool | | SE_16107 | chr2:43405323-43406823 | CD4_Naive_Primary_7pool | | SE_16950 | chr2:43405189-43406902 | CD4p_CD225int_CD127p_Tmem | | SE_17323 | chr2:43404653-43407139 | CD4p_CD25-_CD45RAp_Naive | | SE_17875 | chr2:43395625-43407220 | CD4p_CD25-_CD45ROp_Memory | | SE_18565 | chr2:43400105-43406913 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19552 | chr2:43404989-43406913 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20901 | chr2:43404381-43408464 | CD8_Memory_7pool | | SE_22349 | chr2:43404562-43406734 | CD8_primiary | | SE_23059 | chr2:43404855-43406796 | Colon_Crypt_1 | | SE_23724 | chr2:43404942-43406674 | Colon_Crypt_2 | | SE_24685 | chr2:43404928-43406747 | Colon_Crypt_3 | | SE_26374 | chr2:43404952-43407135 | Duodenum_Smooth_Muscle | | SE_26557 | chr2:43404629-43407112 | Esophagus | | SE_27617 | chr2:43404753-43406882 | Fetal_Intestine | | SE_28536 | chr2:43404713-43407125 | Fetal_Intestine_Large | | SE_30898 | chr2:43405428-43406709 | Fetal_Thymus | | SE_31392 | chr2:43403915-43408015 | Gastric | | SE_33376 | chr2:43404839-43406830 | H1 | | SE_34919 | chr2:43404423-43409363 | HeLa | | SE_38828 | chr2:43404837-43407124 | HUVEC | | SE_40066 | chr2:43404740-43407810 | K562 | | SE_43203 | chr2:43404724-43406909 | Lung | | SE_47826 | chr2:43405061-43406747 | Pancreas | | SE_49954 | chr2:43404447-43406783 | RPMI-8402 | | SE_50052 | chr2:43404769-43406907 | Sigmoid_Colon | | SE_52337 | chr2:43404682-43406959 | Small_Intestine | | SE_53288 | chr2:43405163-43406850 | Spleen | | SE_55101 | chr2:43405389-43406674 | Thymus | | SE_58412 | chr2:43352450-43425007 | Ly1 | | SE_61450 | chr2:43354337-43468354 | Toledo | | SE_62203 | chr2:43354169-43468733 | Tonsil | | SE_65350 | chr2:43405021-43407124 | Pancreatic_islets | | SE_68698 | chr2:43404861-43409084 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I043167 | chr2 | 43394741 | 43409195 |
|
Enhancer Sequence | GAGCTCAGTT CTATGGACTG AGTGGTTCTG TAGACCCAAC AGTGGATAGG GCCAAGACAG 60
GGGGCCTGGG AGATTGTGGA TATCATCACC CCCTGGCCCT GGTGCACTCA TACTCAGTTC 120
TTAAGACCCA GCTCTTTCTG ACTCCTCCAG AAAGACTTCT CTGTCCCTCA GGCTGGGTCA 180
GGCCCCTCAG CGTCCCACTG CACACATGGC AGATAAGTCT TGATCGATGT GCTGTGATAA 240
AGCAGTTATC TGTGTGTACA GCTGGCTCCC CAAGAGACCG TGCCCTCCCT TCTCACTATT 300
CTCTGGAGTC AGGCTCTGTA GCAGCCCAAC ATGGTTTTGA TGAATGAATT AATAAATTTG 360
CTCTGTGATC ATGAGCAAAT TCCCTCTGTC CTGTTCTCAA CAACGGGAAG GCACTATCTT 420
TACTAGATAA GTGAGAGGAA GGGGCCCGGA GGTGGAGGAG GCAGGGCCAG AGGAGGAATG 480
GAGTGGCTCG TGACACCCAC TGTGGGCAGA TGGGATCTGT TAGGAGTGGC TTTGGCTCAC 540
TGGGGCAGGC CAGGGTGGAG AACTGTCACA TACCCTGGTG TACCTCTGGC AAGGAGCTCT 600
GGTGCCATGT GGGAATAGAA GTGCATGGTC CCTTGGCAAG GCTAACGTTT TGTTTTTAAA 660
GAAGTCTGTG TTTCCAGCCT CTTCCTATCT AGTGACCTGG TCCCTGAGAC CTGCCCACCC 720
TCCCGGGCCA TAGCACCAGC CATGCGACCT TGAACCGGTC ACCACTCATC CCTGAACCTC 780
CAAGTTCTCA GCTCTACTGA CAGGGCTGCA GTGCCTTCAT GGGCTGGTGC CTGCCTGGGA 840
GGGAGCCCAG GGATAGAAGC CTGGTTCGCT GGCCACCTCC CGCTGGGGCG TTGGCCCAGG 900
CTGCCAGGTT TCACGTTTCA GCTTTCAGAG TGTTTTCTTG TCTAGGGCAC TTTCTATTTT 960
TCAATACTTT TCCTATCACA GCCAAACAAC AAAAAAGGAA ATTGGTTGAG CCTTCTGAAG 1020
ACCAAGGTCT GGGAGGGTGG GGGTGGGCAG AACCCACCAT GGGAAAAGCT GGAGTCAGGG 1080
CTGAGGGAGG AGAGGCCTCT CCACCCGATT CCCCAGCACC CCTGCTCCCC TTCCTCCGGG 1140
GCTGACTCAT TGTTTTGCAA CAAACAGCCG GCAGCCAGGT CCCAGCAGTT TCTCAAGCCT 1200
GGCCCCCAGG CTGGCTGGGC TCAATCCTGG CCCTCCCAAC TGCCTGGCCA GGCCCTGAAC 1260
GATTGAGTTA TCTCCACTCG CATCCCCTTT GTTTGGGGCG GCTACTTGCC CACTCAAGGT 1320
AAACAAATTC TGGGCCTGTG TGAAAAGAAA GGAACGGTTA TCTCTGAGGC CCTCAGCGGC 1380
CTGGCTGGGG AGCAAGACTT TCAGAGGCTT CTGTCTCCAA AGAGAGGAGG GATTTCGGAG 1440
CATAGCGTCC AGAGGCCAGC TGCCTGGGTT CAAGCTCCAC CTCGGCCACT GACTGCTGAT 1500
GACCTTGGGC AAGTCCCTGA CCTTCTGCTT 1530
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