| Tag | Content |
|---|
EnhancerAtlas ID | HS050-70358 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:127028550-127030300 |
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: 31 | ID | Coordinate | Tissue/cell |
| SE_01861 | chr9:127028027-127030811 | Aorta | | SE_02294 | chr9:127028292-127030548 | Astrocytes | | 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 | chr9:127028617-127030420 | 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: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACTCACTTCA TCCTCCCAGT GATGCCGTGA TGTGGGTATC GTTCTGCCCA TTTTATAGAT 60
GAGGAAACAG AGACCCAGAG AGTCCAGGAT CTGTGGTGCT TGACGAGCAT CAGCCTGAGT 120
GCTGTGAGGA CACCCACAGC ATGGGGGTCT GAGCTGAAAA TTGGAGGACA GAGGCTGCCC 180
TCCGGAAGTG ACCAGGATGT GCCCTCAGGA AGTGACCAGC TGCCCAGCTC AGGACCTGTG 240
TGAGGGCCCC CAGGCAGCTG GAAGGAACAG TGTGCACCCA GGTACCATGC CAGGGCCCCT 300
GAGCATCCGT CTTGTCATCG CATAGTTGTA ACCTGCCTCA CAGACTGAAC ATGCACTCTA 360
GAAGGGGATG GGACTTGGTC TGTGGACCAC AACAGTGTTC TCCATGGCCA GCATTGTGCC 420
TGACACATAG GAGGAGCTCA ATTAATATTT GTTGAGTGAA TGGGAAGTTT TAAGTAGGCA 480
CGCGGCCGGA TCCTTGGAGA ATGTTTATAT GGAGTGAACG AATCTGTTAG CAAACGTTCC 540
TCACTCCCCT CAGTGGGCTG TGCAGGGCTG TATTGAGCTG AGCTGGCCCT TCCCTGGGAG 600
AAGAGGTTTC TTAGAGAAAT GCTCATCCTC GAATTATTCC AATGAGGAGG AACCTAAGCC 660
CAGAAGGGCT CTACCTCCCA GAGTTACAGG CTCTCCTTCC TATGCCCCTT CCCTGCCGAG 720
GCAGCTCCCA CATGTCTGCA TAGGAGGGCT TTGGGTTGGA ATGGGTCAGT GCTGTGTCTT 780
AAAGCTGCAT TTTCTACCAA GCACACACTT TGTTTAGAGG GCATATCTTT TGGGGTTGCT 840
TTGAGGAAAG GCTAACCAAG CCACCTCTGA GCACAGACAT GACTTTTTGG CAAATGAGCA 900
GGACCCCAGA TTACACCCCA TCTTAGAAAG TAGGAAACCC AGCATTGAAA GAGGAAAGAT 960
TCTGCAGCTG ATGTGGCCTT GGCGGGCCAC CAGCGTGGGT GCCCAGATGG CAGGATCACT 1020
GGGCACCACA TGGCACACAG AAGAGAGCAA AGGAGAGGGA GTCCGCCCCT GGGCTTGGCA 1080
GGTCCGGTCG AGTCCGCCTG GATTCAGTTA CAACAGGACC TCGAGTGGGC ACGGCGTGCC 1140
GGACTGAGTC AGTGTGTGTA CATTTCCTTT GTTCGTCTCC TCCGGGAATG TAGTGGCCTT 1200
TTGTGTGTGT TTTAAATGCC AGCCTCCTTA CCTAACCCAA GAGGAAATGA GGACTGGGTT 1260
TTTGTCTGTG CAGACGCTGG GACAAGTGTG GGAGCCGCCT GCTCTTGGAG CCAGCCTAGT 1320
GGTGACAGCG TGGCATTTGG AAAACATTCT GTGGTTTTCT CCAAGGGGTG ATGGGCACAC 1380
CAGGTGCTGG GCCGCCCCTG AGCTGGCCAC TGGGACCCTG AAATGAGGAA GCCCTGTGAC 1440
CAGGTTTCAT GATGCCATTC AGCAAGGGAC GGCTGAGCAC CACATGCCTT CTTGGCCCCT 1500
GGGGAAACAC ACAGGAATCA GATGAGGTCC CTGCCCCGTC TTCCTGGGGA AACATGCAGA 1560
GAAAATACTT GTACTCTGAG CTAACACCTT TCACTCGCAC AGACCTTTAT GGTGTTCTGT 1620
GTCTTCAGAC ATTGATCACC TGTAGGTGAG ACACATCATG GCCCCACTTT CCAAACTCCC 1680
AAACGGGCTG TGATCTGTAG AAGTATTTAG TGCCATTCAG GGACAGGAGA GATGGTTTGG 1740
AAGATGCTGT 1750
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