Tag | Content |
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EnhancerAtlas ID | HS018-00881 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr1:85169910-85171290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr1:85171052-85171063 | TGTGGATTGGA | - | 6.62 | HNF1A | MA0046.2 | chr1:85170909-85170924 | AATTAATGATTTACA | + | 6.76 | HNF1B | MA0153.2 | chr1:85170910-85170923 | ATTAATGATTTAC | - | 6.67 | SPI1 | MA0080.4 | chr1:85170720-85170734 | AAAAAGAGGAAGCT | + | 6.24 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27979 | chr1:85169473-85172789 | Fetal_Intestine | SE_28841 | chr1:85169244-85173420 | Fetal_Intestine_Large | SE_63335 | chr1:85154996-85182414 | NCI-H82 |
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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 |
GH01I084703 | chr1 | 85169245 | 85173420 |
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Enhancer Sequence | GTTCCTTGGA GGTTAAACTG GCAGTTTACT GGAATTGGAA ATTTCCTGAC AATCCAGAGC 60 CCTGGAACAA AATAAGTAGA TATAATAGGC ATCATGTCTG CTATCTTAGA GTGACCATCT 120 TATAACTTAC CCTAGTACAA AAGTTGGACT CTGGAAAGTT TGGGTTCTCA TTTAATGCTG 180 CTAACTAGTT GTGAAATCAT TAGTAAATAA CTCTGGGCTT CATTTTCTTT TTCTGTGAAA 240 TAAATGTGAA TACTTACATT TATTTTGCTT CCCTTCTGCA CAGAAACTCT ATTTGTTCAC 300 GAATTCAACA AATCTCTATG AGCCCTTCCT CTGTACTGGC ACCGTGCAAG GGGCTGGAGA 360 TTCCAAATTG AGTTAGACAA AGTCTCTTCC CTCAAGGAGC CTCTGGGCTG TGAGGATGGT 420 AGGACTGCTT GCTTGTTTGC AGATACTTAA CAATATAAAG TGATAAACGC TGCCACCGAG 480 CTGTGTGGAG GGCATGATGG TAGCTCAGTG GAGATGAGCA TCAAGGTAGA GAAGACTTAC 540 AGAGGAGGAA ACACTTGACT CTTTCTTTCT AGGGGTCTAT TTAATGCTTA AATTTTTTTT 600 CAATTCCATT GCTTAAAAAA ATGAAGTAAT ATATTCATAG AGTATAAAAT TCAAAATGTA 660 CAAAAGGACA TGCTGTGAGA AGCTTCTCTT CTACTCCTCA CCAAGCCACC CAGTTTCTCT 720 TCTCAGGAAC AACCAGGAGT GTCTGTTTCT TGTTTATTCT TTCAGGGACT TGAATTATTT 780 CTTAAAAGAT GTATGCAAGG TACTCAAGTG AAAAAGAGGA AGCTGAGCAT TGCAGACAAA 840 GAGAACAGCA TGAGACTGTT GGGGAGTAGG ACCCATGAGG CGGAAGGCAG TGAGAGAGTC 900 CTCTCCAGGA GGGGCCTTAC CATGCTAAGG AATTTGGATC TGATCCTGAA GCATTAGGAA 960 AGCCATTAGT AGATTTAGAG CAGAGGATCT GCCTGATGAA ATTAATGATT TACAAGGAAC 1020 ACTCTGGCAG AAATGTGAAG AATGGATTGG AGAGAGGCGA GATCAGTGAA AGATACCAGT 1080 TAGGAGGCAA TTGTAATTGT CCAAGGAAGA ACTAATGAGG ACTTAAATCA AGACAGAATC 1140 GGTGTGGATT GGAAGGGGGG CCAACTCTGG TTGTTAAGGA AGAAGGATGA ACAGCATTTT 1200 TGGATCAATT GGATTCCAAT GAATTTAATT CCTGTTCTCT CCTTATCTAA GAATTGCCTA 1260 AGAGTCACAT GCCAAGAATA ATCAGAATTA ATTGCCCTCT CCCTTTAAGC AGTCACCAAG 1320 GCACCCAGTC TTGTCTTAAA TATCTAGCTC AGTGACCTTA AGATATCTAA GCCTCCCAGG 1380
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