EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS116-10156 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr13:111048430-111051050 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs9515203chr13111049623hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXP1MA0481.2chr13:111049553-111049565GTCTGTTTACTT-6.52
FOXP2MA0593.1chr13:111049554-111049565TCTGTTTACTT-6.32
TBX21MA0690.1chr13:111050559-111050569AAGGTGTGAA+6.02
TBX2MA0688.1chr13:111050559-111050570AAGGTGTGAAA+6.62
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00002chr13:111038168-111081448Adipose_Nuclei
SE_01535chr13:111048294-111049328Aorta
SE_01535chr13:111049338-111050444Aorta
SE_01535chr13:111050616-111051201Aorta
SE_02237chr13:111039518-111052677Astrocytes
SE_25773chr13:111039535-111054460Duodenum_Smooth_Muscle
SE_26670chr13:111048390-111049190Esophagus
SE_26670chr13:111049338-111050432Esophagus
SE_29554chr13:111048239-111054354Fetal_Muscle
SE_37003chr13:111039274-111059996HSMMtube
SE_38942chr13:111046463-111049308IMR90
SE_38942chr13:111049346-111051098IMR90
SE_40609chr13:111048350-111051061Left_Ventricle
SE_42124chr13:111048379-111050543Lung
SE_44350chr13:111046226-111051040NHDF-Ad
SE_45553chr13:111039434-111067659Osteoblasts
SE_46823chr13:111048421-111049042Ovary
SE_46823chr13:111049509-111049817Ovary
SE_46823chr13:111049835-111050398Ovary
SE_49078chr13:111048420-111050508Right_Atrium
SE_51324chr13:111046509-111054248Skeletal_Muscle
SE_51789chr13:111047133-111057440Skeletal_Muscle_Myoblast
SE_53243chr13:111048217-111049258Small_Intestine
SE_53243chr13:111049433-111050495Small_Intestine
SE_54480chr13:111035005-111054225Stomach_Smooth_Muscle
SE_56134chr13:111047054-111052503u87
SE_63579chr13:111046443-111057454HSMM
SE_67966chr13:111047054-111052503u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr13111048671111050833
Number: 1             
IDChromosomeStartEnd
GH13I110386chr13111039064111067347
Enhancer Sequence
CTTTAAAGCA GTTCTGGATT TACAAAAACA AAAAAATTAT TCAGAGTGTA CCCATATCCC 60
CTCCCGCTAC CTCTCACCCC TAGTTCCTCC GATTATTAAC ATCTTGTATT AGCGTGCTGC 120
ATTTGTTACA ACTGATACCA GTGTTGGCCT TCCATTATTC TTTTAAATGT GAATCTGACT 180
CTGGGGATTT GTGTGACTGA ATCTCGCAGA TTGAGAACGA TTTTTAACAA CCAGCCATGC 240
TTGTAAAAAC ATGTGGAAGT TTCTCTGACT CTGAAATAAG AGGGACAAGA TGGTTCCCAT 300
GCAGGCTTGC GTTGGAAATG GGGGAGCGTG CACAGTCTAA CTCCATGCCC CGTGTTTTTC 360
TTGAGTAGCC CTCTGGGTTG AATCACCCTG GACTTCAGCT GAGGCAGGGG GATTGTTTTA 420
TGCTCAAGAA AGCTCCAGGA GTGGTAGAAT CTGGCCATCA AGATGTTCTG TGAAATGGGG 480
CTCTTGTCTT TTCTGGAGAA CATGCCTTCT TGGCCCTTTG ATCATGAGAC ATCTCACCAC 540
GCCCTCCTTT AACATTGCTA ATGATGGGGA CTGACCACCC CGTCATTAAA CCCCATGGCA 600
GTCTAAGATT AAGCCATTCA GAATCTTACT AGAAATGACT AAGCGGACCG TTTTTTCTTG 660
TGAGGAGAGA ATTAAAGGCG TTTCCAATCC CTAATGATAA AACCAGCATC AAATTGTAGA 720
GAATTGCAAT TTCTTTCTTA CAAACAGCAA ATTTTTGTCT CCTTTCATTT TTTAAACTGT 780
TGAACGTGTC AGATGGTATG CATAGAGAGA TTTCAGAGGT CTAGTCAATG TGCAAATGTT 840
TTGTGGTTTT ATTTTGAGTT TGAAGTCAGA GCACTGAATT CCACAAGGCT TGAGCCTCAC 900
TCTCCCTCCT GAGCACCCAG GCTTCACGGA CATGACTAAT AGGAGTTTAT TCACAGCCTG 960
CTACCATCCT TGGTCATAAC GTTGCTCAAG GCCCGAGCAG GCCTGCCAAG ACCACAGTGT 1020
AGCCCTGTTA ATATCACATG ACCGTCGGAG AGTTTTTGGA AAACCTCCTC TGGCCGACTG 1080
TTTATCCGCC CCCATTGATA TTTGTCTGAA GATAAGTTAT ACAGTCTGTT TACTTACAAA 1140
TGCGTCAGAA CAGTCTTGGA CTTCTGCACG GAGGTTCTGC CAAATACAAG TCTAACAGGG 1200
AAGTGGTTTG GGCAGCCCCG GAACCGAAGA ACCCCTCAGA GCATCACAAG CCATCACTCT 1260
GGGTCCCTGT CATTTAAATA GGGATTCAGG CTTCAGGTTG TCAGTATTTA TAGGCTTGAT 1320
TGGAGGGAAG TAAGCCGTAT GAGCACTTTT TAAATGAATT TTTATTTCTC ATTTCCACTT 1380
AGTGATGGAT GCACATTTTT CCACTAATAA ACATTTGAAC TTTTTTCAGT TTTTAAGAAC 1440
ATCGTAGGTG GCATATTTCA CAATCTTGGC AAGGCAGACG TTTTTGGAGT AAATCGAAAC 1500
TGGAGGCCAG AAGTACTGGC TCTGAACTGA ACTACCACTT GCAAATCGAT GTAGCAGAAG 1560
GAATAATGGA TCATGTGGAC CACGCAGAAA GCGATCTGAG ACGGGCGTGT CAGCCGCATG 1620
TGGATGAATA GTCCTTTGTG GGCAGGAAGG AGAGGGAGTG GGTGGGTATG AGGGCAGGAG 1680
AAAGAATCAG CTCTGTGTTT GGGGGCTGTG AGAGGACACT CAGAAGAAGG CTTTTACACC 1740
ATATTTTATA TTCACAAGTT TATTTATGTT ATTTTGAGTC CAACAGAAAG AGTCACAAAC 1800
GTTAAACTTT AGCAACCCCC TAATGATTGG AAAAGATGGG CAAATCCTTG CTTTAAGAGC 1860
AGCTGTATCG TATGGAGAAG AAGTCATCTC TGCTGGGAAA ACTCGCGAAC AGATGCAGGC 1920
TAAAGCGAAA GATCAACTCT CCACACCATT ACATTTTGAA GGGCTTTGAA GTTATTTTTA 1980
GAAAAACTCA AAAATCTAAA TCAAAAATCA GATTTTTTCT TTTTTTTTTT CCTACTGCTT 2040
CCTTTTCCTT TTTCTTCTTC TCTTGTCCCT TCTCCTTTTT GGTTGTTTCT ATTGCTATTT 2100
TTACATGTTC CTTTAGGTGG GGGGAAGATA AGGTGTGAAA TGTATTCAAG TGCAACTTTT 2160
TCAAAATAAT AAAATACATG TTTATTATGA GGAAAACTCA ACTGCCTATA GAAATGACAA 2220
CGGTAAATGT AAATAAGCAA AAGATCAGAG ATATAAGTGT ATAGCCATCA CTTCCTTTAG 2280
CAATCAAATA ATGAGCTGGG CGCAGTGGCT CACACTTGTA ATTCCAACAC TTTGGGAGGC 2340
CAAGGTGGGT GGATCAGTTG AGGTCGGGAG TTCAAGACCA GCCCGGTCAA CATGGTGAAA 2400
CCCCGACTCT ACTAAAAACA CAAATGGTGT TTTTAGTGTT TTGTTTTTAG TTTAGTGGTT 2460
TTAGATTTTA GTGGTGGCAA ATGCCTATAA TCACAGCTAC TTGGGAGGCT GAAGCAGGAG 2520
AATCGCTTGA ACCCAGGAGG TGGAGGTTGC AGTGAGCCGA GACCGTGTCA CTGCCCTCCA 2580
GTCTAGGTGA CAGAGTGAGA CTCTGTCAAA AAAGAAAGAA 2620