| Tag | Content |
|---|
EnhancerAtlas ID | HS116-06528 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr11:63640400-63642670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr11:63642163-63642174 | CTAATCCCCTT | - | 6.32 | | Foxd3 | MA0041.1 | chr11:63641107-63641119 | GATTGTTTATTT | + | 6.62 | | PPARG | MA0066.1 | chr11:63640576-63640596 | TAGGGGTGATGGTGACCCAG | - | 6.15 | | RREB1 | MA0073.1 | chr11:63640688-63640708 | GCTGGCTGGGTGGTTTGGGG | - | 7.26 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_03996 | chr11:63640391-63641309 | Brain_Anterior_Caudate | | SE_05069 | chr11:63639184-63642207 | Brain_Cingulate_Gyrus | | SE_06224 | chr11:63639126-63640942 | Brain_Hippocampus_Middle | | SE_06224 | chr11:63641093-63644858 | Brain_Hippocampus_Middle | | SE_08118 | chr11:63639108-63642060 | Brain_Inferior_Temporal_Lobe | | SE_09744 | chr11:63632336-63642538 | CD14 | | SE_23285 | chr11:63639236-63641169 | Colon_Crypt_1 | | SE_23285 | chr11:63641285-63641783 | Colon_Crypt_1 | | SE_24150 | chr11:63640362-63640668 | Colon_Crypt_2 | | SE_24150 | chr11:63640779-63641038 | Colon_Crypt_2 | | SE_26795 | chr11:63639150-63641688 | Esophagus | | SE_26795 | chr11:63641988-63642538 | Esophagus | | SE_27876 | chr11:63639177-63641251 | Fetal_Intestine | | SE_27876 | chr11:63641510-63642406 | Fetal_Intestine | | SE_28858 | chr11:63639200-63641125 | Fetal_Intestine_Large | | SE_31791 | chr11:63639280-63641794 | Gastric | | SE_31791 | chr11:63641820-63642723 | Gastric | | SE_41941 | chr11:63639176-63641138 | LNCaP | | SE_41941 | chr11:63641320-63641775 | LNCaP | | SE_41941 | chr11:63641925-63642515 | LNCaP | | SE_42831 | chr11:63639157-63642663 | Lung | | SE_50305 | chr11:63639072-63641249 | Sigmoid_Colon | | SE_52742 | chr11:63639264-63641184 | Small_Intestine | | SE_65610 | chr11:63640411-63641652 | Pancreatic_islets |
|
| | 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 |
| GH11I063865 | chr11 | 63632968 | 63642725 |
|
Enhancer Sequence | GAGTGACCAG CTCAGAGCGG GACTCAGTCC ACCTCCCTGC TCTGCATGTC AGCAGTGATC 60
TGGAGGAGAT TCCGGGGCGC ATGAGTATGT GAACTCTGGA GCACGTTACT GTCCCGGGCT 120
GGCACTCTGT GGCAGGTGTG TGCACTCATT CTGCTGTTAC TGGAGACCAG TCTCCTTAGG 180
GGTGATGGTG ACCCAGCTAG ATGTCTGCCA GGTCTGTCCA AGGCCACCCT GTTCTCTAAT 240
AGCTTGGGAA ATGGAAAGCA CTTCTAAATA CCCCTGCTCT TCAGAAGAGC TGGCTGGGTG 300
GTTTGGGGAG TTTCTTCTTT GAATCTCTTA GAGTACAATA TCCCTTTTTT CCCGAAAGCC 360
AGGTTCTTTA GTTCCTAAGC TCCATTCTCT TGTTGCTAAC TTACTACCTT CAGTTTTCTT 420
AGGTTGGGTG CATCTTCCCT GGCCTCAACA AGACAGTGGC TGAAAGGTCA AGAGAGTGGT 480
AGCTGCTCCT TTGAGAGAAA GGGGATGTTG GAGTGGGAGC ACAGGCTGCC AGCAGTTGTT 540
TCACCTTCCC CCTTTGGCTG GCTAGGAAAG GGGCACCACT TTAGTCTTCT GCCAACCTCC 600
ACAGCCAGCT GTGGGAAAAC CCAAAAGGAA ACATCCTCTC GCTGCTAAGA CTTGAGAGCC 660
TGAGGCAGAG ACCAGCCAGT AGCAGCCCGA CCCTGCTGAA TGGGGAGGAT TGTTTATTTT 720
ATTTTATTTT TTTCTGAGAC GGAGTCTTGC TCTGTTGCTC ATGCTGGAGT GCAGTGGCGC 780
GATCTCGGCT CGCTGCAACC TCCACACCCC AGATTAAAGC GATTCTTCTG CCTCAGCCTC 840
CCGAGTAGCT GAGACTGCAG GCATGCGCCA CCACGCCCAG CTAATTTTTG TATTTTTAAT 900
AAGAGACAGA GCTTCACCAT GTTGGCCAGG CTGGTCTTGA ACTCCCGAAC TCAGGTGATC 960
CGCCTGCCTC GGCCTCCCGA GGGACTGGGA TTACAGGCAT GAGCTACTGT GCCCAGCCTG 1020
AAGATTGGTT ATTTAGGGGC TGTGACAAAT GGTTTTGCAG AGGAGCACTG GAAAGCCTGT 1080
AACTTCACAG AGCCAGGGGT CAGCTTTTGT GCCATAGCCT TATAGCTTCT GTGGCCTGTA 1140
GTGCCTGAGG CCAGGGGATC AGGTGCTGAC CACCTTTCCC TCTTCCTTCC TGTGTCTTGC 1200
GGCCAGCGAC TGTTATTGTC AGGTTGACCC TCTGGTTAGA GAGGATGACT TTGGCCTGGT 1260
GTCCAGACTC CCTGCTGCCT TATCCCCTCT GCCCTGGAAC TGCACCTAAA AACAATTACT 1320
TTCCTCCTGA TTCCAACATA AGTGGTCACA GAAAGTTCTG TTTTGGCATT TTGATTTCTG 1380
ATTGGGAGTT TAGGCATCTG AGAATTGAAT GCTTGCTTTA TACAAATATA CCCTTAAGAC 1440
ATCTCCTCTT TTTTCAGCCC TACATGCTTT GCTTGGGTAT TAATTGAACT TGGGGCTTTT 1500
TAGGGACCTT ATGTTGCCTA CCTTCCTAGT TTCCCCTCCA CTCCACCCCC AAAAAACCCA 1560
AAGAACATTG GAAAAATTGA GCAGTGCCTC AAGGTCACTT GATCATAAGT GGTATTTGGC 1620
ATAGTTAACT GGTTTGGTGT TTGGTGAGAG ATTTCTGCTT TATATTTGAG CAAAAAATTT 1680
CTTGGCGGGA GGCCTCTATG CTGTGTTGCC AATGCTTGCC CTGTGCGCAG GGTTTGCCCC 1740
CTCCCCTCCC TTGACAGGTT GTTCTAATCC CCTTGTCTAT AAACAAGTGC AGCAGAACTT 1800
GTCGGCCCAG CTCACATGAC CTTGGTTATC TCTTTAACCA GCATCAGCGT TAGATACCAC 1860
GGTCACTTGA CATGGTAGAG CTGTCAGGGT AGAGTGGAGA TACCAGCAGG AATCCTGGTC 1920
CACGAAGAAA GGTAAATGGG AGTGTGTGTG AGGCCTTAGG ACTGGGTGGG AAAAGTCTGT 1980
TCCCATGGGG TAGGGCTTTC AGCTGTGAGA AGAGGATAAT TTCATTCCTT CTCCTTTTTT 2040
AAGAGACTGT CTCACTCTGT CGCCCAGGCT GGAGTGCAGT GGTCTAATCA AGGCTCACTG 2100
CAGCCTCAAC TTCCTTAGCT CAAGCAATCC TCCTGCCTCA GCCTCCTGAG TAGCTGGGAC 2160
CACAGGTGCA TGCCACCATG CCCAGCTAAT TTTTTTTTTT TTTTTTTTTT GAGGTAGAGT 2220
CTCACTCTGT CACCCAGGCT TAAGTGCAGT GGTGCGATCT CGGCTCACTA 2270
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