Tag | Content |
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EnhancerAtlas ID | HS095-06955 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:40619970-40620910 |
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) |
HNF4G | MA0484.1 | chr12:40620232-40620247 | TGGACTTTGAACTCC | - | 7.28 | Hnf4a | MA0114.3 | chr12:40620230-40620246 | ATTGGACTTTGAACTC | - | 7.64 | JUN(var.2) | MA0489.1 | chr12:40620580-40620594 | ATGAGTCACTTTTT | - | 6.86 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_09604 | chr12:40614768-40625158 | CD14 | SE_11539 | chr12:40615334-40628592 | CD20 | SE_61378 | chr12:40602119-40658262 | HBL1 | SE_62819 | chr12:40585765-40628274 | Tonsil |
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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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Enhancer Sequence | GACCCTCATA GTTTGCAACT GTTGTCATAT AAAATGCATG TAGAAGTGAA ACTTTTACAA 60 TCTGTACCAT AGGAAACCCA GAAATTTGCT ATGTATCTTG GATTTTTTTT TAAAGGGGGC 120 CTTAAAAATG GTAATTAAGA ATGATTTACA GTCAAAACAA AATTATAGGC CAAGGTGATA 180 ACTTCCTTCG GAGCACTTAG AGATTTGGGG AACTGAAATC AGTTTTGTCA TCTGCATGTT 240 AACTCATGCA GAGAAAGAGA ATTGGACTTT GAACTCCTTG GAGGTGCAGT CAGAAAGCCA 300 ATGTTTCTTA ATGGTTGAGA GGCTTGACAG ACATGAGGCA TCTCAATCTT TAAAGTGGTG 360 TGGGTCTATC TTTATCTTGA TGTTTATCTC TGTATCTAGC TGTATCTAGT CTGGGTGAAC 420 CATCTAGCTT CTTTGATATG AGGACATTTA CATCTGGAAG AAATATTTTA ATTTGTTTTC 480 AACTGTGAAA TATTTTCCAT CTGACTATTA TAGATTTTCA CGCTGCTATC AAACCAAACC 540 AAGAAAAGAT GGAGGCATAA TAAAGATGCT GTTCTTTTAA GACTCAAAGT CGGAATTTTG 600 CCTGTGGAAT ATGAGTCACT TTTTGGGCAC TGGCCTATTG TGCTTCCTGC TCTGCACCCA 660 CGTCATCCCT TCTTACTTGT CTCTGCTTTG GTGTTCAGAA GTGCCTGATT CTGGCCACCT 720 TCATTCCCTA GACTCTGTAC TTGATAGAGT CACTCCTGCT TGATACTGCT CAGGACAGTC 780 AGATCCTGGG TAGGCGTTTT GGTCTGCAGG GTCTAGATAA GGCAGTGCTA TACTTGACAA 840 CCCAGGGGAG CCTGGAACAT ACTTCCTAAT TCTTAATTTT AGAAATTGCC CAAGCCTGAG 900 CATACTTGTC CGGAGTAGTT ATGAGTGTCA CTTAGTATTT 940
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