| Tag | Content |
|---|
EnhancerAtlas ID | HS146-14932 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr9:38035260-38038050 |
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 | CTATTCAAAG TATAACAGAG TATTTGGGGA GGTAGTGAGC TCCCTGTCAC AGGGGACCTC 60
CAAGCAGAAG CGGGTTGAGC ACTTGGCAAG GAGGACCTAG ACTGAGATCC TTTGCCACTA 120
GAAACTCTAT AGTCCTCCTG AGATTTTTAT GGTACCCTGA AGCATAGGAC TGGGGATAGG 180
GGAGCCAGTG TTGAAGGGGT TGCTCCAACC TTATAAAACT GCATCCCTCC CTCTCACTTT 240
CACAGGCTGC TCAGTGAGAG AGGTTCTCCA CCTCTTTCCC CAGTGGCATG TGAAAGGTTG 300
GGTGCCATGG GAGAAGCACA GAATCACATC CTGAAGTTCA GCAATGCCCA CGGTGGGGTA 360
GGTCTTGGGG ACAGAAGGAC AAAGCTCAGT CAGTGTCTAC CTTCCATGAG TGGATAATCT 420
AGGGAGAGGT CAGCAACCCT CTCCTGTAAA TTACCATATA GAAAATATTT TAGGTTCCTG 480
AGGGTCATAC AGTACTCCTG GTTTAGTCCA GTGATTCTCA ACATAGCTGC ACATCAGAAA 540
AACTCCTGGG GAGCTTTTAC AATGCACCAT GCCTAAGTTT GGCCCCCAGA AATTCTGATT 600
TAAGTGGCCC AAGGTGGGGC CTGGGATTAG TATTTCTAAA AGCTCCCCTA GGAGCTTGGA 660
TACAATCCAT CCAAGACTGA GAATCACTCT CTGGTCTCCA GCAGAAACAG GCGCGTGCAA 720
AACCTCAGCA TTATCCCCAG TGATTTCCCA AACCCAGCGA GGGGAAGTGA CTCGCTCAAG 780
GTCATACAGT GAGTCAAGAG GCAAAGAATC TGAGCCCAAG ATCTTCTCCC TGCAGCACCC 840
AGGCACAGAC AGGCCCAAAC TCCTGTTCCA GAGCTTGGGA TACCAGGCCT TCTTGCTCAA 900
GCCCTGCTGC CCCATAAGGT GAAGACCCCA GAGAAACACC AGCCACATTC GCCCCGACCC 960
ACTCTAACGC ATGGGGCACT GCCCTCTCTC CAGACCAAAC CTCAACGAGG TAGAACTAAC 1020
AGGGGAATGA ATTTCTAAAA CAGCCACATT TTAACCAAAA TTGCTAACAG TTTATTAGCA 1080
TCTGGGAGGA ACAAAAGTTA GGGCTGTAAA AACTGTATTT CTTCAGTCCT AACAAGCGCA 1140
GCCACAGCAA ACTCTTTACC AATGACACCA CTAAAGACTT GCCAAAACGT GCCGCCTGCC 1200
TAGAGCTCTG CCCACGCAGG ACTTGGGCAC AAGGAACCCC CAGAGCCCTT GGGAATGTTG 1260
CAAGAGCTTG GCTGAGGCTG GGTGGCCACT GGCGGCGATG ATCTCAACGT CTACAGAGCA 1320
AATGAGCTCC GAAAGACAGG GCAGACCCAG GCATCCCCCG CCTAGCAGGA GCTCTGCTAG 1380
TGGAGATAAC TGGAGAGTCT CTGAGCCCCA GACTCTCTGG GGTTCTCTCC ATTGAGCCAC 1440
AGGACAGTGA GGGACTTGAG AGAGCAAGGA TGGGAGAAGC TGAATAATAA TACAAGAAAT 1500
ACTGAGAGCA GCTACCAGGG ACTATGCTCA GTTCTTTTAA TACAACATCC CTATGGATTT 1560
GATTCTCATA TTGTCCCCAT TTTACAGATG AAAAAAACCA AGGCATGGGG TGGCTGGATA 1620
ACATGTCCAA GGTCACCAAA GCAGTTAAGT TGCAGAGCCC TGACTCAAAC TCGGGTGCTG 1680
TCTCTTAATC TTATGCTCAA CAGACTTAGA AGTGACTCTA CTATGAAACT CCTCCCTGCA 1740
GAGACAGCAA AATAGACCCA GAGAGAGCAA GGGACTGGTG CAGGACCCCG CAGCACGGGA 1800
GCTGGGGTAA AAGCAGTTCT GTGTACTGCC CTGTAGACAG CCTGGCTTTG GGCCCTACTA 1860
GGCTGACACA ACTCCCTCTT TTCCCGGAGA AGAATCCTGC GATCTCCTTA TGACACAACA 1920
GTGGGCTCAA ACAAGAGAAC TGGAGAAAGA GATGGCACAC AGGGCTCTTG TCTGTAGTCT 1980
GTGTAAAGTA CCAATTGCTG GAGTACTCCG TGTCATTTGG AAACTTCCTA TCTTACCTCC 2040
ATATAGGCCC ATGGTCAACA GGGCTGTGAG CTTGTTTCCG ACACCTGCCC CCACCACTGC 2100
CCGCTCCAGT CACACGCAGA GTCACCAGCC CCCAACTTCC CCAGGGGGTC TTCACTCATA 2160
CTGTGCCCTT CTCTCTTCTC TGATCACTGC ATGTTCAAAT TCTATCTAAC CTCCAATGCT 2220
CGGCACATGA GAACATGAGC TCTAGAGTGA AATGTGGGTT GAAATCCACA CTGTGTCACC 2280
TTGAGAAGTT TGCTCAACCT CTCTGGGCCT CAGTTTCTTC ACTATAAAGT GGGGATAGTA 2340
ACAGAACCCA CCTCAGTGCT TGGCAACAGG AGGGGCTCAA CTGTGTGTCA TTATCATCGA 2400
TTCAGCCCCC ATGTACCATT CTGAGAACCC CACCTCCGCT AGAAGTGAGC CTCTCTCCTC 2460
TGAGCCCTGA AGTTCTGTCT GCTCCTCCAT TCAGCCTCCC TGGGCTGACC TTGGGGCAGA 2520
TCCTGTGCTG GGCTCTGGAA CATAGAGCAG AAGGAGTGGT CCTTCCTGCA GGAGACACAG 2580
GCTCATTGGG GGATAGCCAC AGGCTCACAA ATAGGCATGA CACAAGGTGG CTGGGCTAGA 2640
AGAGGAGCTA AAAAGTGACA TTTCACATTC TGTCACACTC TAACAAGATT TTTTTTAAAA 2700
TCTGGCTCTC TTCCTACTGA CTAAAAGTGG TTTAACTAAC TCCTAACACA TTGTCTAAGA 2760
GTTTTTAAAA GTCAGGCCAA ACTCTATTTG 2790
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