| Tag | Content |
|---|
EnhancerAtlas ID | HS094-42644 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr9:38035370-38037880 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr9:38036035-38036046 | TCAAGGTCATA | + | 6.62 | | Esrra | MA0592.2 | chr9:38036034-38036045 | CTCAAGGTCAT | + | 6.02 | | Esrrg | MA0643.1 | chr9:38036035-38036045 | TCAAGGTCAT | + | 6.02 | | PRDM1 | MA0508.2 | chr9:38035493-38035503 | TCACTTTCAC | + | 6.02 |
|
| | Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
| SE_00446 | chr9:38035274-38037855 | Adipose_Nuclei | | SE_01843 | chr9:38035849-38037381 | Aorta | | SE_02310 | chr9:38035164-38037218 | Astrocytes | | SE_04803 | chr9:38037075-38038316 | Brain_Cingulate_Gyrus | | SE_05785 | chr9:38036275-38041022 | Brain_Hippocampus_Middle | | SE_23246 | chr9:38034914-38035808 | Colon_Crypt_1 | | SE_26555 | chr9:38035522-38037321 | Esophagus | | SE_27864 | chr9:38029824-38035624 | Fetal_Intestine | | SE_28791 | chr9:38029759-38035765 | Fetal_Intestine_Large | | SE_33929 | chr9:38035258-38037356 | HCC1954 | | SE_34811 | chr9:38034088-38040783 | HeLa | | SE_36884 | chr9:38035316-38037082 | HMEC | | SE_38030 | chr9:38034960-38040717 | HUVEC | | SE_38998 | chr9:38035048-38039881 | IMR90 | | SE_40993 | chr9:38037427-38040848 | Left_Ventricle | | SE_42283 | chr9:38037522-38040704 | Lung | | SE_44329 | chr9:38035017-38039025 | NHDF-Ad | | SE_44779 | chr9:38035042-38040081 | NHLF | | SE_45758 | chr9:38034875-38040105 | Osteoblasts | | SE_47196 | chr9:38029911-38057164 | Panc1 | | SE_48861 | chr9:38036997-38040800 | Right_Atrium | | SE_51847 | chr9:38035299-38037355 | Skeletal_Muscle_Myoblast | | SE_55662 | chr9:38034844-38039953 | u87 | | SE_57367 | chr9:38035126-38035751 | VACO_503 | | SE_57367 | chr9:38036342-38036769 | VACO_503 | | SE_63571 | chr9:38035287-38037494 | HSMM | | SE_64986 | chr9:38035005-38037312 | NHEK | | SE_65279 | chr9:38035619-38036887 | Pancreatic_islets | | SE_65279 | chr9:38037547-38039359 | Pancreatic_islets | | SE_67542 | chr9:38034844-38039953 | u87 |
|
| | 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 |
| GH09I038035 | chr9 | 38035151 | 38041531 |
|
Enhancer Sequence | TTTGCCACTA GAAACTCTAT AGTCCTCCTG AGATTTTTAT GGTACCCTGA AGCATAGGAC 60
TGGGGATAGG GGAGCCAGTG TTGAAGGGGT TGCTCCAACC TTATAAAACT GCATCCCTCC 120
CTCTCACTTT CACAGGCTGC TCAGTGAGAG AGGTTCTCCA CCTCTTTCCC CAGTGGCATG 180
TGAAAGGTTG GGTGCCATGG GAGAAGCACA GAATCACATC CTGAAGTTCA GCAATGCCCA 240
CGGTGGGGTA GGTCTTGGGG ACAGAAGGAC AAAGCTCAGT CAGTGTCTAC CTTCCATGAG 300
TGGATAATCT AGGGAGAGGT CAGCAACCCT CTCCTGTAAA TTACCATATA GAAAATATTT 360
TAGGTTCCTG AGGGTCATAC AGTACTCCTG GTTTAGTCCA GTGATTCTCA ACATAGCTGC 420
ACATCAGAAA AACTCCTGGG GAGCTTTTAC AATGCACCAT GCCTAAGTTT GGCCCCCAGA 480
AATTCTGATT TAAGTGGCCC AAGGTGGGGC CTGGGATTAG TATTTCTAAA AGCTCCCCTA 540
GGAGCTTGGA TACAATCCAT CCAAGACTGA GAATCACTCT CTGGTCTCCA GCAGAAACAG 600
GCGCGTGCAA AACCTCAGCA TTATCCCCAG TGATTTCCCA AACCCAGCGA GGGGAAGTGA 660
CTCGCTCAAG GTCATACAGT GAGTCAAGAG GCAAAGAATC TGAGCCCAAG ATCTTCTCCC 720
TGCAGCACCC AGGCACAGAC AGGCCCAAAC TCCTGTTCCA GAGCTTGGGA TACCAGGCCT 780
TCTTGCTCAA GCCCTGCTGC CCCATAAGGT GAAGACCCCA GAGAAACACC AGCCACATTC 840
GCCCCGACCC ACTCTAACGC ATGGGGCACT GCCCTCTCTC CAGACCAAAC CTCAACGAGG 900
TAGAACTAAC AGGGGAATGA ATTTCTAAAA CAGCCACATT TTAACCAAAA TTGCTAACAG 960
TTTATTAGCA TCTGGGAGGA ACAAAAGTTA GGGCTGTAAA AACTGTATTT CTTCAGTCCT 1020
AACAAGCGCA GCCACAGCAA ACTCTTTACC AATGACACCA CTAAAGACTT GCCAAAACGT 1080
GCCGCCTGCC TAGAGCTCTG CCCACGCAGG ACTTGGGCAC AAGGAACCCC CAGAGCCCTT 1140
GGGAATGTTG CAAGAGCTTG GCTGAGGCTG GGTGGCCACT GGCGGCGATG ATCTCAACGT 1200
CTACAGAGCA AATGAGCTCC GAAAGACAGG GCAGACCCAG GCATCCCCCG CCTAGCAGGA 1260
GCTCTGCTAG TGGAGATAAC TGGAGAGTCT CTGAGCCCCA GACTCTCTGG GGTTCTCTCC 1320
ATTGAGCCAC AGGACAGTGA GGGACTTGAG AGAGCAAGGA TGGGAGAAGC TGAATAATAA 1380
TACAAGAAAT ACTGAGAGCA GCTACCAGGG ACTATGCTCA GTTCTTTTAA TACAACATCC 1440
CTATGGATTT GATTCTCATA TTGTCCCCAT TTTACAGATG AAAAAAACCA AGGCATGGGG 1500
TGGCTGGATA ACATGTCCAA GGTCACCAAA GCAGTTAAGT TGCAGAGCCC TGACTCAAAC 1560
TCGGGTGCTG TCTCTTAATC TTATGCTCAA CAGACTTAGA AGTGACTCTA CTATGAAACT 1620
CCTCCCTGCA GAGACAGCAA AATAGACCCA GAGAGAGCAA GGGACTGGTG CAGGACCCCG 1680
CAGCACGGGA GCTGGGGTAA AAGCAGTTCT GTGTACTGCC CTGTAGACAG CCTGGCTTTG 1740
GGCCCTACTA GGCTGACACA ACTCCCTCTT TTCCCGGAGA AGAATCCTGC GATCTCCTTA 1800
TGACACAACA GTGGGCTCAA ACAAGAGAAC TGGAGAAAGA GATGGCACAC AGGGCTCTTG 1860
TCTGTAGTCT GTGTAAAGTA CCAATTGCTG GAGTACTCCG TGTCATTTGG AAACTTCCTA 1920
TCTTACCTCC ATATAGGCCC ATGGTCAACA GGGCTGTGAG CTTGTTTCCG ACACCTGCCC 1980
CCACCACTGC CCGCTCCAGT CACACGCAGA GTCACCAGCC CCCAACTTCC CCAGGGGGTC 2040
TTCACTCATA CTGTGCCCTT CTCTCTTCTC TGATCACTGC ATGTTCAAAT TCTATCTAAC 2100
CTCCAATGCT CGGCACATGA GAACATGAGC TCTAGAGTGA AATGTGGGTT GAAATCCACA 2160
CTGTGTCACC TTGAGAAGTT TGCTCAACCT CTCTGGGCCT CAGTTTCTTC ACTATAAAGT 2220
GGGGATAGTA ACAGAACCCA CCTCAGTGCT TGGCAACAGG AGGGGCTCAA CTGTGTGTCA 2280
TTATCATCGA TTCAGCCCCC ATGTACCATT CTGAGAACCC CACCTCCGCT AGAAGTGAGC 2340
CTCTCTCCTC TGAGCCCTGA AGTTCTGTCT GCTCCTCCAT TCAGCCTCCC TGGGCTGACC 2400
TTGGGGCAGA TCCTGTGCTG GGCTCTGGAA CATAGAGCAG AAGGAGTGGT CCTTCCTGCA 2460
GGAGACACAG GCTCATTGGG GGATAGCCAC AGGCTCACAA ATAGGCATGA 2510
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