Tag | Content |
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EnhancerAtlas ID | HS176-20561 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:54813080-54814780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr2:54813463-54813474 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr2:54813463-54813474 | GGTGACTCATG | + | 6.02 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00006 | chr2:54811575-54819309 | Adipose_Nuclei | SE_00896 | chr2:54814579-54815214 | Adrenal_Gland | SE_07789 | chr2:54813346-54816182 | Brain_Inferior_Temporal_Lobe | SE_11005 | chr2:54790737-54825699 | CD20 | SE_12885 | chr2:54814124-54818971 | CD34_Primary_RO01480 | SE_13387 | chr2:54812274-54819355 | CD34_Primary_RO01536 | SE_14098 | chr2:54814276-54819273 | CD34_Primary_RO01549 | SE_15859 | chr2:54812306-54814574 | CD4_Naive_Primary_7pool | SE_17333 | chr2:54793892-54821363 | CD4p_CD25-_CD45RAp_Naive | SE_18341 | chr2:54795035-54821330 | CD4p_CD25-_Il17-_PMAstim_Th | SE_21502 | chr2:54812192-54813951 | CD8_Naive_7pool | SE_21966 | chr2:54805854-54819252 | CD8_Naive_8pool | SE_22380 | chr2:54811304-54814282 | CD8_primiary | SE_22380 | chr2:54814371-54819185 | CD8_primiary | SE_27627 | chr2:54814586-54819090 | Fetal_Intestine | SE_28537 | chr2:54811085-54813333 | Fetal_Intestine_Large | SE_28537 | chr2:54814445-54819018 | Fetal_Intestine_Large | SE_38000 | chr2:54811565-54818799 | HUVEC | SE_39396 | chr2:54811057-54819524 | Jurkat | SE_40773 | chr2:54813450-54814305 | Left_Ventricle | SE_40773 | chr2:54814413-54816146 | Left_Ventricle | SE_42137 | chr2:54814409-54816036 | Lung | SE_46220 | chr2:54812024-54814377 | Osteoblasts | SE_49907 | chr2:54809659-54819600 | RPMI-8402 | SE_50115 | chr2:54814479-54816047 | Sigmoid_Colon | SE_53342 | chr2:54813620-54814093 | Spleen | SE_53342 | chr2:54814421-54816087 | Spleen | SE_60008 | chr2:54784446-54818579 | Ly4 | SE_61167 | chr2:54784367-54847020 | HBL1 | SE_61474 | chr2:54749764-54818736 | Toledo | SE_62304 | chr2:54783676-54846716 | Tonsil | SE_66257 | chr2:54811057-54819524 | 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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| Number: 1 | ID | Chromosome | Start | End |
GH02I054584 | chr2 | 54811564 | 54820841 |
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Enhancer Sequence | AATGAAGAAT ACTCTGTGAG AAGTGAAATT TTGAGTTACA CATTGGGATA TGATATCACT 60 TAGAAAATAG TGCTAAACTT TAAAATTCTT TAGTTTCAGA ATTTTCTAAA TCAGGGAGGG 120 GCTTGTCAGT ATAAAATTAT ACATTTTGTT TTTTGATCTT GTCACAGTTG TTCGTGACTT 180 CTGAAATCCA AGTGTGGTTT GGAGACGACT TTACCCCACT CCTCCCCAAA CACACATTGG 240 TAGTCCGTGG CTTACTTGCG TAGACAACTG TGATTGTGGA GTTTGGCACT CGAATTGAGA 300 CAGTCGTATT TAATTTATCA ATCTGTCGTT TCAACCCTGA ACTTTTCTAC AATGGGTTAT 360 GGTCACTGGC CAAAAAGGGT TTAGGTGACT CATGTGTAAT GTTCTTCAGA ACAGAAGCCA 420 ATTTTTAAAT CCTTTTGTAT TTATGTTCAT TTATTTTTAA ATATAATTCC TCTTCTCATT 480 AAGTGGAATC TTGTCATAAT TCTATAGTTT CAAGTGATAA CTTGGCATTG CTGTGGCTTT 540 CTTTATTCCA AAATGCTAAT CCTTTGCAGA TAAATTTATA CATTCTGTAT AGTCTGATTT 600 GGAGGACTTC TGTATCTTAG CTTATCTTAG ATGGGAGCTT CCATAATTCA TTCAGGGATT 660 AGTCAGTGCT ATACTGTGCA TGCATAGTAG ACAGCTCTGT GTGGTGGCTT TAAGTCTTTT 720 GACTCCCCCT CTTTCTGGTC TTTGTGTCTT TCTGGTTTAA AAGAAAAAAT ATCCCTCAGA 780 CCTTAGCTTT TTGGATTCAA TGAATTACTG TTAACTTTGA CATCCTCATT AAATAGGAGA 840 GCTGTCGGAA ACTGTCAAGA ACGGCTGGAA TTGGTACTGT TATCTTGTTG GCGACGTCAG 900 CTTCTGTGGG CATCTGTGCA AAAACATTGA GGTAGAGCAG AATCCTCTTC TATCTTGAAT 960 GTCTGAAAAT AATGTGACTG GTGTGTTTGA AAGAGTTCTA TTTTTCCCTC TTTGCCCTTA 1020 ATTATTTTGG CCTTAAGGAT TCCGGAAACC TGGAGTAGAT TGAAAACCAT AATAAGCAAG 1080 GGCCGGGGAG CATGTTATTT GATTTTTTAA TAAACTACCT CTGACTAGCT TACACGCCCC 1140 GTAGAACATT AAGGCTACTT TTTGTGTATA TTGCATGAAA TAAGAAACAT CACAAATTTG 1200 AATTCTCTCT CAATACCTCT GCTTTATCCA AGGCTCCTAC AACAAAAGCC TACCTTTAGC 1260 CCTTGAAAAT GAAGTAGAGG ATTTTATCTT TACTGGTGAA TTTGTGTGCC ACATGGTAGA 1320 CTAGTATAGA ATGTAATATT TACTGCTTCT TTAATGTTCC TTAGGAAGAA TATCACACAG 1380 ACATCTCCCT TCTCCATATG TTGCAATTAT ACTACTTTCA TGAAGTCTTG AGTGTGCCTG 1440 TTACGGTTGG TGCGCTTTAA AACATTCTTT TCTACTTAGT CTGTATTCGT GTTAACGTTC 1500 TGCCATTCTG TGTTAAGTTC TGCCGTTCTG TGTTGTTTAG TAATTAAGTG TATGGTATCT 1560 ATTTAGTTCT AAGTTTTTCC TAACTTTTAA GGGCATTGCA AGTTACCCTC AGCCCACCTT 1620 GGATTGAAGT CCCCTTCCAT GGAGGACTGG AGGAGAAGAG GTGATGGTGT ATGAAGTGTC 1680 CATCAAAATA AGAGCTGAAG 1700
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