Tag | Content |
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EnhancerAtlas ID | HS148-03248 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr11:65886290-65887920 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr11:65887786-65887801 | TGAACTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_11071 | chr11:65886060-65888898 | CD20 | SE_17686 | chr11:65886229-65887631 | CD4p_CD25-_CD45RAp_Naive | SE_58381 | chr11:65834101-65902512 | Ly1 | SE_59665 | chr11:65833534-65914414 | Ly4 | SE_62408 | chr11:65835434-65906336 | Tonsil |
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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 |
GH11I066111 | chr11 | 65878489 | 65888783 |
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Enhancer Sequence | AGCTTATTTT CTCGTTATTT CCTTCTCTCC CTTCCCAAAT ATTTTTTTGA GCATCTGTGT 60 CAGCTAGGAA TACAGAAACT AAAAAACATT GCTTGCCCTT GTGACTGGGG AGATATAGAC 120 AATTGAATAA TCAACCACAA CATGTTATAG TAAGTGCTAA GATAAAGGTA GGCACAAGTG 180 TCAGGGAAAA CACAGAAGTG GGATGCCTGA GCTGAGTGGG AGTGGGGGTG GCCCAAGAAG 240 GCTTCCTGAA CCAGTGGCAC CAGATGGACA AGGGAGAGGC CCCCTACTCC CTGCTTGTCC 300 TCTGCTCTCT TCTGACCGGT AGCGTTAATA CTTCTTTGGT TTAATGCAGG ATCACCAGAC 360 TCTGTGGCCC ACGACCTGTT TTTGTGTAGC CCATAAGACA TACCTTTCTA AGTACTATAG 420 CTGAAAAACA TCAAAAGAGT AGTAATATTT TGTGACATGT GAAAATTATA TGAAATTCAA 480 ATTTCTGTCT GTAAACCTCA CTGGAACACA GCCATGCTCA TTCGTTTGTA TATGGTCTGT 540 GGCTGCTTTC TCCCTACAAC GGTAGAATTG AACAGTTGCA TCAGAGACCT TATGGCCTGC 600 TAGGCCAGAA ATGTTAAGCC CTTTACAGAG AAAGCTTGCT GGCTCCTGTT TAATGCTTTA 660 ACTGCCCTAC TGAAAGGCAG GAGGTTGAAA AAATGATGGT AGTCAAAAGG AATGCATGAA 720 ATCCTGTTGT CTTCTGTTAG CTGATTGCAA GTAGTACACA GGATATATTT GAGACATCTC 780 TTTTCCTATC TCCCACCAAA GGATAATTCA GGCGGATCTC AGTGCACAGG CACAGGCATT 840 TGCCTCATTC TTGTTTTGTC TGTTTTGAAT TTAGTTATGG GAATATTTTA ATATCTCTCA 900 AAAATAGGGT ATCTGGTGTG AGTCAGAATG ATTATAGAAC ATGCTTGCCT GGAGAACAGG 960 AAATGCGGGA TCCACTCCTG GTGTGCTGTT AGCTGAAGGA CGTCAGAACT GTCCTTTAAC 1020 CTCCCTGCAG GTCTCTAAAT GGTAGGATTG TTTGGGGATT ACACTAGATC ATCTCTAGGC 1080 ACCGTTCAGC TCAGTAGAGA CATTGCTGCA TGGTGGAAGG AGTGACCTCA GTGTGAATCC 1140 TGGTTCTGTC CCTTTCTGCC CAGGAGACCT TGAGCAGCTT ATCTAAATGC TGTGTGCCTT 1200 TGTTAGCTCA TCTGAAAATG TGGCTGTAAG AATGACCTCA TGAGAATGGA CTGAGATCAT 1260 ATTCTTAAAA CTCTTGGCAC TAATAGGTAT TTAATCTACT ATAACTGTGA AAATTATGTC 1320 TGTGAACTCT TTTTTTTTTT TTTTTTGAGA CAGAGTCTCG CTCTGTTGCC CAGGCTGGAG 1380 TGCAGTGGCA CGATCTCGGC TCACTGCAAC CTCTGCCCCC TGTGTGCCAC CACTCTCGGC 1440 TAATTTTTGT ATTTTTAGTA GAGATGGGGT TTCACCATTA TTGGCCAGGC TGTTCTTGAA 1500 CTCCTGACCT CAAGTGATCC ACCTGTCTTG GCCTCCCAAA GTGCTAGGGT TACAGGCGTG 1560 AGCCACTGGA CCCAGCCTGA ATACTAATTA TATACTTCAT TTTAATCAAA CTCAATTTGT 1620 GAAATAGCTG 1630
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