| Tag | Content |
|---|
EnhancerAtlas ID | HS116-00494 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:19740560-19741990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr1:19741093-19741108 | GGCTATTTTTGGTTT | - | 6.3 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_00361 | chr1:19739675-19741018 | Adipose_Nuclei | | SE_01631 | chr1:19740052-19742151 | Aorta | | SE_02919 | chr1:19741493-19741875 | Bladder | | SE_03519 | chr1:19741082-19741860 | Brain_Angular_Gyrus | | SE_04046 | chr1:19739390-19741938 | Brain_Anterior_Caudate | | SE_05077 | chr1:19739768-19742310 | Brain_Cingulate_Gyrus | | SE_05833 | chr1:19739893-19742257 | Brain_Hippocampus_Middle | | SE_07251 | chr1:19739724-19742317 | Brain_Hippocampus_Middle_150 | | SE_08066 | chr1:19739884-19742462 | Brain_Inferior_Temporal_Lobe | | SE_18410 | chr1:19740631-19742057 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_25786 | chr1:19739366-19746495 | Duodenum_Smooth_Muscle | | SE_26537 | chr1:19738055-19747014 | Esophagus | | SE_28668 | chr1:19740060-19741985 | Fetal_Intestine_Large | | SE_29645 | chr1:19739644-19744492 | Fetal_Muscle | | SE_31447 | chr1:19739717-19740970 | Gastric | | SE_31447 | chr1:19741288-19741879 | Gastric | | SE_41031 | chr1:19740477-19741922 | Left_Ventricle | | SE_42185 | chr1:19740033-19741997 | Lung | | SE_45720 | chr1:19740827-19741772 | Osteoblasts | | SE_46635 | chr1:19740460-19741101 | Ovary | | SE_46635 | chr1:19741104-19742017 | Ovary | | SE_48688 | chr1:19739984-19742053 | Right_Atrium | | SE_50058 | chr1:19737847-19743255 | Sigmoid_Colon | | SE_51211 | chr1:19739125-19745063 | Skeletal_Muscle | | SE_52345 | chr1:19740021-19742118 | Small_Intestine | | SE_53453 | chr1:19740292-19741803 | Spleen | | SE_54550 | chr1:19737698-19742888 | Stomach_Smooth_Muscle | | SE_65446 | chr1:19740101-19741226 | 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 |
| GH01I019413 | chr1 | 19739347 | 19747479 |
|
Enhancer Sequence | ATGGGCTGCT TCACGGAGAG CAGGTTTTTG GAAACGTAAG CAGCGGGTGT CCACTCACTC 60
GTTCACTAAG GCTCGAATGT GGACACGTCC CCCAAGCACT CAGCCTTCTC ATCTGTCAAA 120
TCACACTCCC TGCAGACATC ATGCTGCCCC GATGGGGGTG GCGATGCGGG GGTGACAGGG 180
ATAATTTCAA AGCATGGCTA CCGCTGAGGC TGGCAGTGTG AATACCTGTG CCCAGCTGGC 240
TCTATTTCTA GAGGGCTGCT CTGGCTACTT AAAAAGAAGA ATATGCTGAA AACAGTTAAC 300
CTATGAAGTT ATCAACTCCC CGGTAAAAAA TCAGGATGTC TCTTCCACCT TTACCTCACT 360
GGCCTGGATA CTTTCCCAGC CCTGATGTCT TCCCCTTGAT AGAGTAAAGT CTGGGGACAC 420
CCAAGAGCTG AGCCTTAGGA CAACTGTAAG AAAGAAAGAA GTGAAGGAAC TAAAAACATG 480
AAGTGACCAA TGTTTGCAAG CAGAGACTTT CTTGCCTAGT TAAACAGATT CACGGCTATT 540
TTTGGTTTGC TCTTAAAAAG GCAAAGGATG GAAGGCCTGC TGGGTGCCAA TATGCAGAAA 600
CAAACTCCTT CCTCAGCTCA GGGCTCAAAA TACACCCCAG CTGAGACATT TCTGCTCTTG 660
CTGCCAGTGT GCAGAGTAAG GCCATAGAAG GGCCAAGTTT ATGAAGCCAA GGGAACATCT 720
TCACATCATA TGATTCTTGG CCCTCATGGA TGTGTGGGTA TTTTTGAAAC AGCTTAACAA 780
CGGATTTCAG CTGGATTCAC TCTAGCACAA TGGGATTAAT ATGTAATAAA ATGATGTTTT 840
GGCCATCTGC AAAGGAAGGT CATTTCCCAC CAATCAGAGC AGGCCTCATA ATCCCAAGGC 900
AGCAAAAACT CTCTGATGCT GGGAAGAAAA AAGAAAGCTG ACCTGGCATG ATAAATTGGG 960
CTGCCTTGGC CTGGCTGCCA AGCATCCCTC ACATTTCTCT TCAATACCAC TCTGTAATCA 1020
GACCATGGTG GACTGGATCC ATTCCCCCAC AGTTCCCTGG CCCTGACATC TTAAGCGAGG 1080
CCATTCCCTT CATGGGGAAT GCTGGCAAAT CCTAACATTC TCGTCCATCT TAAAACTGGA 1140
GACTTTTCTT GAAAACAACA ATCTCCCCCC CTTCATTATC TTGGGCAGGT GAGCAGGGAG 1200
GAATGACTGC TGTTTGCATG GAGCAGCAGT GCATTAGCTA CTTTCAAAAC ATCTGACTGA 1260
TCCCAGATTA CACGAGACAA AGGCCTGGAT CCTTTGCCTT TAGACAGGTG CATAATAGTG 1320
TGAATTTTCT GAAACTACCG CTTTGGGAAG AAACTAAAAC TGCATGTGAA CTTCAATGCT 1380
ACAACAGTAT ACTCAGCACA GACCAATCCT TACAGAATAA AAGCATTTCG 1430
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