| Tag | Content |
|---|
EnhancerAtlas ID | HS105-83155 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr9:127027820-127030430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gabpa | MA0062.2 | chr9:127028731-127028742 | CCGGAAGTGAC | + | 6.14 | | RUNX1 | MA0002.2 | chr9:127029896-127029907 | TTCTGTGGTTT | + | 6.32 |
|
| | Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
| SE_01861 | chr9:127028027-127030811 | Aorta | | SE_02294 | chr9:127028292-127030548 | Astrocytes | | SE_03002 | chr9:127027842-127028520 | Bladder | | SE_04593 | chr9:127028891-127030342 | Brain_Anterior_Caudate | | SE_06625 | chr9:127028933-127030320 | Brain_Hippocampus_Middle | | SE_09789 | chr9:127025946-127031287 | CD14 | | SE_23712 | chr9:127027894-127031158 | Colon_Crypt_1 | | SE_24006 | chr9:127027853-127028277 | Colon_Crypt_2 | | SE_24006 | chr9:127028279-127028609 | Colon_Crypt_2 | | SE_24006 | chr9:127028617-127030420 | Colon_Crypt_2 | | SE_26169 | chr9:127028464-127031167 | Duodenum_Smooth_Muscle | | SE_27460 | chr9:127028546-127029502 | Esophagus | | SE_27460 | chr9:127029577-127030298 | Esophagus | | SE_29975 | chr9:127028907-127030325 | Fetal_Muscle | | SE_31765 | chr9:127027836-127031189 | Gastric | | SE_36996 | chr9:127027502-127031245 | HSMMtube | | SE_38009 | chr9:127027450-127031685 | HUVEC | | SE_38868 | chr9:127028106-127031763 | IMR90 | | SE_42506 | chr9:127027674-127031138 | Lung | | SE_44293 | chr9:127028727-127031058 | NHDF-Ad | | SE_44809 | chr9:127028276-127028828 | NHLF | | SE_44809 | chr9:127029011-127029548 | NHLF | | SE_45648 | chr9:127018281-127031420 | Osteoblasts | | SE_47283 | chr9:127027822-127030793 | Panc1 | | SE_47557 | chr9:127029471-127030049 | Pancreas | | SE_50283 | chr9:127027697-127031101 | Sigmoid_Colon | | SE_51779 | chr9:127028340-127030620 | Skeletal_Muscle_Myoblast | | SE_52726 | chr9:127027715-127030348 | Small_Intestine | | SE_54297 | chr9:127028449-127030673 | Spleen | | SE_59258 | chr9:127016097-127031007 | Ly3 | | SE_60141 | chr9:127018983-127030974 | Ly4 | | SE_60448 | chr9:127019058-127056389 | DHL6 | | SE_63558 | chr9:127028209-127030812 | HSMM | | SE_65907 | chr9:127028092-127030478 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 127028281 | 127028331 | | chr9 | 127028725 | 127030267 |
|
Enhancer Sequence | GTCTTGCTTT AAAAAAAAAA ATACCTCTCC TTTTACAGAT GGCGACACTG AGGCCCAGAG 60
AGACATCATG ACCAGCCTCA GGTCCCACAT GCAGCCTGCT GCTCTGTAGC CTAAATCAGA 120
TCACTGTCCC AGCTTTCAGG TCAAGGCTCT GGTTGTGACA CCTGGGCCTG GACTGCGGGT 180
GAAAAGTTTT GATGCAAAAA CACAGACCGT CCATTGTCCT ATGGGCTAAG TGGACTCCCT 240
TCTGCTAACC AGAGATGCTT GTGCTGGCTG GTGTGTGGCA CGTTATCTCA TTCTTTCATG 300
ACGTATGTCC GGATGGAAGT CCTGGGTCAG GCATTGTGCT GGGAGCCCAC ACGAAGACCC 360
TCTAATGGCC CCACCCATTG GCCTCTCACC ACCTGGTGGG GACAGAGGCT GTCACAACCC 420
CTTCTTAGGT GCTCTTGATC AATTTGCAGG TGGCATTTTT TGGGATGTAG TCTCTGGGGA 480
AGTAGGAGAG CTTCCGGCAG TGAGGGGTGT TTGAACCCAC CTGGAGGGAG ACGTGGGGTT 540
TGCCAGAGGG CTGAGAGGGC TGGGGTGAAG GGCAGGTAGA CCCCAAGGTG GAGAGGCAGG 600
TGGGGCCGGT GGGTGAGAGG TGGGGCTGTG GAACTTCCTC CTGCTTCTTT GGCCTTTGCT 660
CCTGTCGGTA GATGGCCTTA CCAGGCACTT ACTGTGGGCC ATGTTCTAAT CTAACCCTTA 720
ACCTGAGGGA ACTCACTTCA TCCTCCCAGT GATGCCGTGA TGTGGGTATC GTTCTGCCCA 780
TTTTATAGAT GAGGAAACAG AGACCCAGAG AGTCCAGGAT CTGTGGTGCT TGACGAGCAT 840
CAGCCTGAGT GCTGTGAGGA CACCCACAGC ATGGGGGTCT GAGCTGAAAA TTGGAGGACA 900
GAGGCTGCCC TCCGGAAGTG ACCAGGATGT GCCCTCAGGA AGTGACCAGC TGCCCAGCTC 960
AGGACCTGTG TGAGGGCCCC CAGGCAGCTG GAAGGAACAG TGTGCACCCA GGTACCATGC 1020
CAGGGCCCCT GAGCATCCGT CTTGTCATCG CATAGTTGTA ACCTGCCTCA CAGACTGAAC 1080
ATGCACTCTA GAAGGGGATG GGACTTGGTC TGTGGACCAC AACAGTGTTC TCCATGGCCA 1140
GCATTGTGCC TGACACATAG GAGGAGCTCA ATTAATATTT GTTGAGTGAA TGGGAAGTTT 1200
TAAGTAGGCA CGCGGCCGGA TCCTTGGAGA ATGTTTATAT GGAGTGAACG AATCTGTTAG 1260
CAAACGTTCC TCACTCCCCT CAGTGGGCTG TGCAGGGCTG TATTGAGCTG AGCTGGCCCT 1320
TCCCTGGGAG AAGAGGTTTC TTAGAGAAAT GCTCATCCTC GAATTATTCC AATGAGGAGG 1380
AACCTAAGCC CAGAAGGGCT CTACCTCCCA GAGTTACAGG CTCTCCTTCC TATGCCCCTT 1440
CCCTGCCGAG GCAGCTCCCA CATGTCTGCA TAGGAGGGCT TTGGGTTGGA ATGGGTCAGT 1500
GCTGTGTCTT AAAGCTGCAT TTTCTACCAA GCACACACTT TGTTTAGAGG GCATATCTTT 1560
TGGGGTTGCT TTGAGGAAAG GCTAACCAAG CCACCTCTGA GCACAGACAT GACTTTTTGG 1620
CAAATGAGCA GGACCCCAGA TTACACCCCA TCTTAGAAAG TAGGAAACCC AGCATTGAAA 1680
GAGGAAAGAT TCTGCAGCTG ATGTGGCCTT GGCGGGCCAC CAGCGTGGGT GCCCAGATGG 1740
CAGGATCACT GGGCACCACA TGGCACACAG AAGAGAGCAA AGGAGAGGGA GTCCGCCCCT 1800
GGGCTTGGCA GGTCCGGTCG AGTCCGCCTG GATTCAGTTA CAACAGGACC TCGAGTGGGC 1860
ACGGCGTGCC GGACTGAGTC AGTGTGTGTA CATTTCCTTT GTTCGTCTCC TCCGGGAATG 1920
TAGTGGCCTT TTGTGTGTGT TTTAAATGCC AGCCTCCTTA CCTAACCCAA GAGGAAATGA 1980
GGACTGGGTT TTTGTCTGTG CAGACGCTGG GACAAGTGTG GGAGCCGCCT GCTCTTGGAG 2040
CCAGCCTAGT GGTGACAGCG TGGCATTTGG AAAACATTCT GTGGTTTTCT CCAAGGGGTG 2100
ATGGGCACAC CAGGTGCTGG GCCGCCCCTG AGCTGGCCAC TGGGACCCTG AAATGAGGAA 2160
GCCCTGTGAC CAGGTTTCAT GATGCCATTC AGCAAGGGAC GGCTGAGCAC CACATGCCTT 2220
CTTGGCCCCT GGGGAAACAC ACAGGAATCA GATGAGGTCC CTGCCCCGTC TTCCTGGGGA 2280
AACATGCAGA GAAAATACTT GTACTCTGAG CTAACACCTT TCACTCGCAC AGACCTTTAT 2340
GGTGTTCTGT GTCTTCAGAC ATTGATCACC TGTAGGTGAG ACACATCATG GCCCCACTTT 2400
CCAAACTCCC AAACGGGCTG TGATCTGTAG AAGTATTTAG TGCCATTCAG GGACAGGAGA 2460
GATGGTTTGG AAGATGCTGT CTGCTGTGCG AAGTCTCTGG ATGCTCAAAT GGCTTATGGG 2520
GTGGCATCTT TGAAATTACC CAGTCCTGAA AATTTCAGGA CATATGGTCA CTGTGATGTG 2580
CTAATGTTAG CAATTGAGAT ATTTAATGAC 2610
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