Tag | Content |
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EnhancerAtlas ID | HS129-11639 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr14:61822140-61823180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr14:61822931-61822951 | TGCAGTGGGTTGTTTGGGGG | - | 6.03 | Sox6 | MA0515.1 | chr14:61822903-61822913 | CCATTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr14:61822851-61822872 | GAAAGAGGAAGTGGAGGGGGG | + | 6.65 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_17300 | chr14:61820539-61826153 | CD4p_CD25-_CD45RAp_Naive | SE_18232 | chr14:61806323-61826750 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19137 | chr14:61821208-61823400 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19991 | chr14:61822078-61823438 | CD56 | SE_22282 | chr14:61787293-61826617 | CD8_primiary | SE_38197 | chr14:61820856-61826421 | HUVEC | SE_62242 | chr14:61787351-61886567 | Tonsil |
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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 |
GH14I061354 | chr14 | 61821235 | 61824105 |
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Enhancer Sequence | TTTAAAAACT GTTAGCTCCT TGAGGGAAGG GATAGTGTGA TCTTTTGGTA GGAGACTTTA 60 AAAGATCCAC TTTCTTATAT TTTAGTGTAT CCCTTGGGTC AAATGGAGGA TTTTTTTTTA 120 AAGGATGATC ATCAAATAAA TATTTTAAGT AATTTGACCA AAATTTATCT TCTTACCTTT 180 TTACTAAAAA TATACACTAA ATAATTTTAA GGGAAGATTT TATAGTCTCA TATTCAACAT 240 GGAAATTTCT TGATTAGTAT TGCCCTGACT TTATTGGTTG CTTCACGGGT GGCTTCTGAA 300 TTCATTTCTT GGAATGTTAC TATTCAGGGC CAACTTTGTT AGTATTGCTA CGTTGTGATT 360 TAATTTTTTG CCACTTACAC ATTCTAGCCA GTCTGGAAGA TCTCCACCAA AACACCTGTA 420 TAGTTCAGTC TGAATTTAGA AGTGTCACTT GCAAGAGAGG CAGCAACGTC AGGCCCGTGA 480 GACTCAAGAG AAGTCTCTTT CCATGATAGA TCTTCTTATA CTTGGTAGAA ACTGGCAAGT 540 GACTCACCAG GGGTGGAAGC CTGGAAAACA GCCTGCCGAG GAGGGTAGTC TTTCTGGTAA 600 CACATCGCCA CCCCTTTGAA GCATCCAGAG AACCGGAAGA GCAGGAACTG CCTGTCAGAC 660 TGACTGAGCG CTTGGCATTC TTTCATGGAA AGATGACAAC TCATCCAGGG TGAAAGAGGA 720 AGTGGAGGGG GGTGGCAGGG AACAGGAGGG TGACCTTACA TTTCCATTGT TTTGCAGGCT 780 GCCTGGTCGA GTGCAGTGGG TTGTTTGGGG GTTGGGAGGA ATTGGAATCA TGTACTTCTA 840 TTGTTGCTGT CCAAAGTGGA TGTCCTGTGC TGTGTTGCCA AGGAGGGGAG CTTGTACCCA 900 TTTTATCCTT GTGCTCCTTC GTAATCCAGA TGGTTTGTGA TCTGATATTT CTTTCGTGCT 960 TAGCCCTGGA CTCTATCGGT TAGAATCCTA GTATCATTTT AAGAACTGGG ATTCTCCTAT 1020 GCCAAATTTC TGTGAAATCT 1040
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