Tag | Content |
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EnhancerAtlas ID | HS148-00022 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr1:2177400-2178460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:2178443-2178458 | AAGGTCAGGAGTTCA | + | 6.04 | Zfx | MA0146.2 | chr1:2177478-2177492 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_11007 | chr1:2177126-2179681 | CD20 | SE_17322 | chr1:2177380-2179108 | CD4p_CD25-_CD45RAp_Naive | SE_20071 | chr1:2177580-2178390 | CD56 | SE_41586 | chr1:2177735-2178477 | LNCaP | SE_46124 | chr1:2177298-2178497 | Osteoblasts | SE_62490 | chr1:2120386-2191742 | Tonsil | SE_68979 | chr1:2177579-2181412 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 2177405 | 2178400 | chr1 | 2177615 | 2177829 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I002245 | chr1 | 2177240 | 2183861 |
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Enhancer Sequence | AATTTTTGTT TTTTTAGTAG AGACGGGTTT CGCCACGTTG GCCAGGCTGG TCTCTGACTC 60 CTGGCCTCAA GCCGTCATCC CGCCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCGTGAGC 120 CACCGCATTC AGCCCGTTTT TCTTTTTAAA GAACCGACTG TTTTTCATAG TGGCTGCAGC 180 ATTTTCCACT CCCAGCAACA GCGTTCGAGC AGCACTGTCT TTGCATCCTC TCCAGCACTT 240 GTTCTGTTTT TTGACAGCGG CCATCCTAAT GGGTGTGAGG TGGCATCTCA TTGTGGTTTT 300 GGTTCTCATT TCCCTGATGA TTAGTATGTT GGGCATTTTT TCGTGTGCTT ATTGGCCACT 360 CCTATATCCT CTTTGAGGAA TGTCTGAGTC CCTCTTTGAG TCGAGTTGTG TGTGGGGGCC 420 TTTGCTCAGT TGTACGTCTT TATCTACTCT GGTTAGTGAT CCTGTTCTAC TTGTAAATTT 480 CTGTCTCCTG TTTGTCTACT GCGTGCACCG TGGTCGGATC CTGCCTCTGT TGCTGGAGGC 540 TGCCTCTGTC CTCTGCTGTG GTGGTCAGGA AGCTGGAGCG TCTCGGCGCC AGATTCATGT 600 TTGTAAGAGG AGACGCTCTG TGAGCCTCGG TGTGCAGCGC TGTCTGCAAG TCAGACTCCC 660 CACCCCTCCT TTGTGCGAGC TGGGCGGGGG CTCTGCCGGG ACTGGTGGTG TTCATGGAGA 720 GGGCTTCTGT GTGATGAAGA GATGACAGTG ACCTGCTGGG GCCGAAGGCT GTGAGTGCCA 780 TTGGGGGAGG GAGTCTCAGA GAGTGCGGCA GTCGGGCCTG ATGGGGCTGC TCTTCTGTGA 840 AGGGGCACCT ACCGTGTGCC TGGCCTGTAG CAGCAGCAAA GAGGAACCTG ATGGGGGGGG 900 CCTCAGGAAC CTCCACCTCG CCCACTGTGG CCAGGCTGCT TCTGCTTTCT GGGAGGCCTG 960 TGCAAGAGCC ATGGGCACAG GCCGGGCACG GTGGCTCACG CCTGTAATCC CAGCACTTTG 1020 GGAGGCTGAG GCCAGCGGAT CACAAGGTCA GGAGTTCAAG 1060
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