Tag | Content |
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EnhancerAtlas ID | HS034-20045 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr22:41050420-41051590 |
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) |
Nfe2l2 | MA0150.2 | chr22:41050836-41050851 | CTGCATGACACAGCA | + | 6.19 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_64695 | chr22:41049954-41051335 | NHEK |
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| 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 |
GH22I040650 | chr22 | 41046877 | 41051796 |
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Enhancer Sequence | TGTTTTCCTT TTTTTAAGAT AAGAGTTATA TAGTAACTCA GAGCTCAGTA ACATCAGCAT 60 TTTGGAAGTA GGATAGGAAG AAAGTCTCAT CACAAGGGAG CCCTGTGGAG AGGAATGAGC 120 ACAGAATTTG GAGTCAGAAG AGTGGAAGGC CTGGGCTTGG GGCCTGGCTG CACCGTGCCG 180 GCTGGATTGT TCTGGGAAAG CTGCCCAACT CTCTGCTCCG CAGTCCCCAC ATCTGTCACT 240 AGGGATCATA TCTGCCTCAC AGGATCAGCT GAGATAAGGC ACGTGTGTAA AAGGCTGTAC 300 AAATGTTAGT TACTATAAGG TTGTCTCAAA AAAATAAAAC CCACGGCAAA GAGTATCCCA 360 AGGCAGGCTC ATTTTACTCC AATTACCATT TGGCACCGAG CAGATCAGGG GACTTACTGC 420 ATGACACAGC AAGTCAGTGG AAGAGCCAAG GAGTGCACTC ATCCAAGTTA CTGATTCCGA 480 TGTCAGCAAA ACCTGCTGAA ACCCATCTTC ACACTGCAGT TCAGAGGGTG TCCCCAGGAA 540 GCACCTCTCT GCAAAGCATG TTCAACGTAG TTCCCAGTGG CCTGCCAAAT GGTCAGCAGC 600 AAGGTGTAAC TGGATGTCGC TTCCAGGAAG CAGAGTGAAA AGAGACAAGG AGTAGGAAAC 660 TAATGTCCAG AGTCGGCCAT TTGCCCCAGG GACCGGAGTG GAGACTGCAT TTCTAAGTGC 720 TTCCTCTGTC CACAGCCCTC CTCCCCCATA CCTTTTAAAA ACAGATTTGC TGGCTGGGTA 780 CGGTGGCTCA TGCCTGTAAT CCCAGCACTT TGGGAGGCTG AGGCAGGTGA ATTGCCTGAG 840 CTCAGGAGTT CGAGACCAAC CTGGACAAAA CCCTATCTCT AGCAAAAAAT ACAAAAAGTT 900 AGCCGGGCCT TGTGGTGCAT ACCTGTGGTT CCAGCCACTG GGAAGGCTGA AGTGGGAGGA 960 TCACTTGAGC CTGGGAGGTG GAGGTTGGAA TGAGCTGAGA TTGCGCCACT GCACTCCAAC 1020 CTGAGTGACA GAGTGAGACC CCATCTCACA AAAACAAAAC ACAGATTTGT TGGCTGGGCA 1080 TAGTGGCACA TGCCTGTAAT CCCAGCACTT TGGGAGGCCG AAGCGGAAGG ATCACTGGAG 1140 TCCGGGAGTT TGAGACCAGC CCAAGCTGTG 1170
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