| Tag | Content |
|---|
EnhancerAtlas ID | HS155-00197 |
Organism | Homo sapiens |
Tissue/cell | Ovary |
Coordinate | chr1:19740500-19741990 |
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 | TGACTAATAG TATCATCCTT AACGTCACCA GTCAATTACA AATGTGTGTG AGCTGGCTCC 60
ATGGGCTGCT TCACGGAGAG CAGGTTTTTG GAAACGTAAG CAGCGGGTGT CCACTCACTC 120
GTTCACTAAG GCTCGAATGT GGACACGTCC CCCAAGCACT CAGCCTTCTC ATCTGTCAAA 180
TCACACTCCC TGCAGACATC ATGCTGCCCC GATGGGGGTG GCGATGCGGG GGTGACAGGG 240
ATAATTTCAA AGCATGGCTA CCGCTGAGGC TGGCAGTGTG AATACCTGTG CCCAGCTGGC 300
TCTATTTCTA GAGGGCTGCT CTGGCTACTT AAAAAGAAGA ATATGCTGAA AACAGTTAAC 360
CTATGAAGTT ATCAACTCCC CGGTAAAAAA TCAGGATGTC TCTTCCACCT TTACCTCACT 420
GGCCTGGATA CTTTCCCAGC CCTGATGTCT TCCCCTTGAT AGAGTAAAGT CTGGGGACAC 480
CCAAGAGCTG AGCCTTAGGA CAACTGTAAG AAAGAAAGAA GTGAAGGAAC TAAAAACATG 540
AAGTGACCAA TGTTTGCAAG CAGAGACTTT CTTGCCTAGT TAAACAGATT CACGGCTATT 600
TTTGGTTTGC TCTTAAAAAG GCAAAGGATG GAAGGCCTGC TGGGTGCCAA TATGCAGAAA 660
CAAACTCCTT CCTCAGCTCA GGGCTCAAAA TACACCCCAG CTGAGACATT TCTGCTCTTG 720
CTGCCAGTGT GCAGAGTAAG GCCATAGAAG GGCCAAGTTT ATGAAGCCAA GGGAACATCT 780
TCACATCATA TGATTCTTGG CCCTCATGGA TGTGTGGGTA TTTTTGAAAC AGCTTAACAA 840
CGGATTTCAG CTGGATTCAC TCTAGCACAA TGGGATTAAT ATGTAATAAA ATGATGTTTT 900
GGCCATCTGC AAAGGAAGGT CATTTCCCAC CAATCAGAGC AGGCCTCATA ATCCCAAGGC 960
AGCAAAAACT CTCTGATGCT GGGAAGAAAA AAGAAAGCTG ACCTGGCATG ATAAATTGGG 1020
CTGCCTTGGC CTGGCTGCCA AGCATCCCTC ACATTTCTCT TCAATACCAC TCTGTAATCA 1080
GACCATGGTG GACTGGATCC ATTCCCCCAC AGTTCCCTGG CCCTGACATC TTAAGCGAGG 1140
CCATTCCCTT CATGGGGAAT GCTGGCAAAT CCTAACATTC TCGTCCATCT TAAAACTGGA 1200
GACTTTTCTT GAAAACAACA ATCTCCCCCC CTTCATTATC TTGGGCAGGT GAGCAGGGAG 1260
GAATGACTGC TGTTTGCATG GAGCAGCAGT GCATTAGCTA CTTTCAAAAC ATCTGACTGA 1320
TCCCAGATTA CACGAGACAA AGGCCTGGAT CCTTTGCCTT TAGACAGGTG CATAATAGTG 1380
TGAATTTTCT GAAACTACCG CTTTGGGAAG AAACTAAAAC TGCATGTGAA CTTCAATGCT 1440
ACAACAGTAT ACTCAGCACA GACCAATCCT TACAGAATAA AAGCATTTCG 1490
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