| Tag | Content |
|---|
EnhancerAtlas ID | HS095-30772 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr9:38035360-38037600 |
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: 27 | 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_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_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 | ACTGAGATCC TTTGCCACTA GAAACTCTAT AGTCCTCCTG AGATTTTTAT GGTACCCTGA 60
AGCATAGGAC TGGGGATAGG GGAGCCAGTG TTGAAGGGGT TGCTCCAACC TTATAAAACT 120
GCATCCCTCC CTCTCACTTT CACAGGCTGC TCAGTGAGAG AGGTTCTCCA CCTCTTTCCC 180
CAGTGGCATG TGAAAGGTTG GGTGCCATGG GAGAAGCACA GAATCACATC CTGAAGTTCA 240
GCAATGCCCA CGGTGGGGTA GGTCTTGGGG ACAGAAGGAC AAAGCTCAGT CAGTGTCTAC 300
CTTCCATGAG TGGATAATCT AGGGAGAGGT CAGCAACCCT CTCCTGTAAA TTACCATATA 360
GAAAATATTT TAGGTTCCTG AGGGTCATAC AGTACTCCTG GTTTAGTCCA GTGATTCTCA 420
ACATAGCTGC ACATCAGAAA AACTCCTGGG GAGCTTTTAC AATGCACCAT GCCTAAGTTT 480
GGCCCCCAGA AATTCTGATT TAAGTGGCCC AAGGTGGGGC CTGGGATTAG TATTTCTAAA 540
AGCTCCCCTA GGAGCTTGGA TACAATCCAT CCAAGACTGA GAATCACTCT CTGGTCTCCA 600
GCAGAAACAG GCGCGTGCAA AACCTCAGCA TTATCCCCAG TGATTTCCCA AACCCAGCGA 660
GGGGAAGTGA CTCGCTCAAG GTCATACAGT GAGTCAAGAG GCAAAGAATC TGAGCCCAAG 720
ATCTTCTCCC TGCAGCACCC AGGCACAGAC AGGCCCAAAC TCCTGTTCCA GAGCTTGGGA 780
TACCAGGCCT TCTTGCTCAA GCCCTGCTGC CCCATAAGGT GAAGACCCCA GAGAAACACC 840
AGCCACATTC GCCCCGACCC ACTCTAACGC ATGGGGCACT GCCCTCTCTC CAGACCAAAC 900
CTCAACGAGG TAGAACTAAC AGGGGAATGA ATTTCTAAAA CAGCCACATT TTAACCAAAA 960
TTGCTAACAG TTTATTAGCA TCTGGGAGGA ACAAAAGTTA GGGCTGTAAA AACTGTATTT 1020
CTTCAGTCCT AACAAGCGCA GCCACAGCAA ACTCTTTACC AATGACACCA CTAAAGACTT 1080
GCCAAAACGT GCCGCCTGCC TAGAGCTCTG CCCACGCAGG ACTTGGGCAC AAGGAACCCC 1140
CAGAGCCCTT GGGAATGTTG CAAGAGCTTG GCTGAGGCTG GGTGGCCACT GGCGGCGATG 1200
ATCTCAACGT CTACAGAGCA AATGAGCTCC GAAAGACAGG GCAGACCCAG GCATCCCCCG 1260
CCTAGCAGGA GCTCTGCTAG TGGAGATAAC TGGAGAGTCT CTGAGCCCCA GACTCTCTGG 1320
GGTTCTCTCC ATTGAGCCAC AGGACAGTGA GGGACTTGAG AGAGCAAGGA TGGGAGAAGC 1380
TGAATAATAA TACAAGAAAT ACTGAGAGCA GCTACCAGGG ACTATGCTCA GTTCTTTTAA 1440
TACAACATCC CTATGGATTT GATTCTCATA TTGTCCCCAT TTTACAGATG AAAAAAACCA 1500
AGGCATGGGG TGGCTGGATA ACATGTCCAA GGTCACCAAA GCAGTTAAGT TGCAGAGCCC 1560
TGACTCAAAC TCGGGTGCTG TCTCTTAATC TTATGCTCAA CAGACTTAGA AGTGACTCTA 1620
CTATGAAACT CCTCCCTGCA GAGACAGCAA AATAGACCCA GAGAGAGCAA GGGACTGGTG 1680
CAGGACCCCG CAGCACGGGA GCTGGGGTAA AAGCAGTTCT GTGTACTGCC CTGTAGACAG 1740
CCTGGCTTTG GGCCCTACTA GGCTGACACA ACTCCCTCTT TTCCCGGAGA AGAATCCTGC 1800
GATCTCCTTA TGACACAACA GTGGGCTCAA ACAAGAGAAC TGGAGAAAGA GATGGCACAC 1860
AGGGCTCTTG TCTGTAGTCT GTGTAAAGTA CCAATTGCTG GAGTACTCCG TGTCATTTGG 1920
AAACTTCCTA TCTTACCTCC ATATAGGCCC ATGGTCAACA GGGCTGTGAG CTTGTTTCCG 1980
ACACCTGCCC CCACCACTGC CCGCTCCAGT CACACGCAGA GTCACCAGCC CCCAACTTCC 2040
CCAGGGGGTC TTCACTCATA CTGTGCCCTT CTCTCTTCTC TGATCACTGC ATGTTCAAAT 2100
TCTATCTAAC CTCCAATGCT CGGCACATGA GAACATGAGC TCTAGAGTGA AATGTGGGTT 2160
GAAATCCACA CTGTGTCACC TTGAGAAGTT TGCTCAACCT CTCTGGGCCT CAGTTTCTTC 2220
ACTATAAAGT GGGGATAGTA 2240
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