Tag | Content |
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EnhancerAtlas ID | HS182-19685 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:30292310-30293680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr7:30292666-30292680 | AGGAAGTGACTCAG | + | 6.23 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_58314 | chr7:30198366-30326987 | Ly1 |
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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: 3 | ID | Chromosome | Start | End |
GH07I030252 | chr7 | 30292521 | 30292817 | GH07I030253 | chr7 | 30292981 | 30293170 | GH07I030255 | chr7 | 30293221 | 30293370 |
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Enhancer Sequence | AAGGAAACTG ATATGGAGAA ATATATTATT TTGACAAGTG TTTCTTGGGC ATCTACTATC 60 TCCATATATG ACCCAGTTGC CCCTGAGAGC TAATTCCAAC TACATGGAGA TGCTCACGAT 120 CAATGATGAG ATGGCATGGT GCATGAGAGT CAGGGAACAG TCTTCAAAGC TCAACACAAC 180 CAGCTGTGGC TTTCACTTCA CTTGAATTAG GTCATAGAGT CATAACCTGT AAAATGAGCA 240 ACTTGGACTA GACTACCTCC CTGGTCAGCT TCAAGACGCC ACGGCTATAC TTCCATTTCA 300 GAACCAGGCC CCATGGAGTG TGTGGTTGCT TAGACAGCCT CAGTAAGTCC CCGTCTAGGA 360 AGTGACTCAG CCATGTCAGT GTGGGGCTCA CACCCCAACA GGCTTCCCAC TCCTTGCTGC 420 ACCAGTCTTC ACCCCAGACC TAGGCCCTCT GGGTGGGGTG GAGCTCCTTC CCAGTGTTCC 480 CTCCCTTCTC CTTCTGCCCA CCTCAGATCT ACCCTTTGTC ACTTGCCTAC TGAGACCAGC 540 CAACTTGAGG CAATCATTCC TGCCAAGTTA GCCAGTGGCT GCATATATCA TACTCAAGGC 600 AACATTCTTA TGGTAAAAAT TTACTTTCTG CAGATACCAA CCCTGGTAAA GTCTCCAATT 660 TATTTCCTAC AACAACTAAC CTTCTCACAT TCTTTGTTTC AGCCTCAAGG GCAGTTCCTG 720 GAATTCACCA GGCTCTTCAC TGCCCTCAGC CTTGGCCTCT AGCCAATGCT GCTGCCACTG 780 CCCAGAAATC TTCTCCTCCA CTCAGCACTC TGTTAACTCC TTTCCGCCCT TCAGCAACAG 840 CTTCCAAGTC TCTTTCCCCA ACTGAGCCCT CTGCTATTCT CTTTTCCGTC ATAGATCTTA 900 GCAGAAAGTA CAAACATCTC CCTCAGTAGA TGACAGATTT CATGAAGGCA CTGTGCCACC 960 GTACACCTGG TACCTGCCTG GTACACAGCA GGGGCTCAGG TTAATAACCG TTGGTTAAAT 1020 ACATGGATGA ACAAATGAAT GAAAGCACTG TCTTAACCCA AAGATGAGAC AGATGGTAGG 1080 AATTGCAGGC CCTGGCACAT GTCGATGGGG GAAAGAGACA TTTTTGAGCA GGTGAAACTT 1140 GTCTCTTATC TCTACCTGCA GTGCTCACCT GACTCCTGAA GGACAGACAC TAGCAGCAGA 1200 AAATATCATC ACTCCCAAAT GTAGCTTGTC CTATAACTGT TTGTCAACAA TAAGGCTTTG 1260 ACTCACTACA AAAGCTTTCT TCACATGAAT TCAAAGCATT TTGCTTTGCA TTTGAGCAAG 1320 CCTGTTGGTG ACAGCAGTCC TTAGAATGTG AAGCACAATG GTTTAAACAT 1370
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