Tag | Content |
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EnhancerAtlas ID | HS080-03317 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:230864360-230865620 |
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) |
NR2C2 | MA0504.1 | chr1:230864918-230864933 | TGCCCTTTGACCCCC | - | 7.16 | Nr2f6 | MA0677.1 | chr1:230864918-230864932 | TGCCCTTTGACCCC | - | 6.46 | Rxra | MA0512.2 | chr1:230864918-230864932 | TGCCCTTTGACCCC | - | 6.73 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_32194 | chr1:230864487-230865515 | Gastric |
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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 |
GH01I230728 | chr1 | 230864231 | 230865816 |
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Enhancer Sequence | ATGCTGCCAC TTACTGAGAA CTTTTGAGGT ATGGGTCACC CTTTTAAGCT TTTGCATCTA 60 CGGCCTCATT TTCATGCTTT GTAACAGTGT CCACAGCAGC ATACAGAGAA GGGGAGAAAA 120 GGTTTGTGTG TACTCTTTGC ACCATAGCTC TTTCAGCACA TGCATTAGTT TTGCTCTTGC 180 CTCACATCCT CTTTTACTAA TGCCAGGAAA CACATCCAAC ACAACCTTAT ACTCCCTGCA 240 ATCCCTGTCT CATGGGAGTA GAGAATCCTC ATAGTGAGGA TTGAATTAGT TAACATATGA 300 AAGCATTTGG AGCAGAGCCT GCCAGGCAGT GAGCCCTGGG AGAGCATTAG TTGCTATATC 360 ACTCGTGAAA AGCCTTCCGG AAATGTGGTT GTCCACTAGG AGACTGAGCA AAGACAGTCA 420 GGTACCCATG CAGTTAACTC AGTCAGGCTA ACAGCAAACA GAACTTCAAA GGCCACCTGA 480 CCCTCTCCCC TGACCCAGAA AGCCTGAGGC ACCTGCCTGG TGCAGTTTCT CCACCATCTG 540 CCATGCAGGG CACCACCATG CCCTTTGACC CCCACCTTCC ACTCTCTCTC TGGACTTTCA 600 TCCGCACTCA GCAACAGCCT GTTGGCGCCA AACAGCCTCC AGCCCTAATT GCTCTTCCTA 660 GCTCCCGGGC AGTGTTCCCA ACACCTAGTA GCCACTGTAA GGACAAATGC AACTTAAAAA 720 CAAGAGGCTT AATTCTCCCG GTTGAAAATG GGGGAAGAGG TTTCCCTCCC TCTCTTATTC 780 TCAGAGCATT TACCTTAGAA AACTTGTAAT TATAAGCACT TTCTCCTCTC TTTCAAATGT 840 ATATAACATT TTTGTGAAGA TCAGAGAGGA CTTTTGTCAG CTTGATTACC CAGGCATGTG 900 TTTCTCAAGG ACCCGGGAGC CATCTCCTTG AAAGGCAAAC ATCAAGGGAG AGACAGTGGC 960 CCCAGCTCCC AGTGTCTGTG GGAGGGTGAC AGCCTGCCTT CAGTGGGCAC ATGCCTCCAA 1020 GCTGCAAAAC TGCCTCCTGT CACAAAGATG TAAGAAGCTT GTTTTTCTCT AGATAAAGCC 1080 CATTAGCTAA TACAGATGGT CACCTCAGTT GCCAGGTAAA GTTAGAATGA GCTGTGTGTG 1140 ACAAGTAGTG TTGTCAAGTT CTCTTACTAC TTATGTCACC CAGTGTAATG CCTACATGAC 1200 ATAGCTGAAT TTCTACTCTT CTCTAACCTG TCTTCTCTAT CTTATCTTTA AGAAACAGGA 1260
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