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

TagContent
EnhancerAtlas ID
HS116-08389 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr12:57525530-57528350 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11172113chr1257527283hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr12:57526979-57526999TGTGTGTGGCTGGGGTGGGG-6.39
RREB1MA0073.1chr12:57527408-57527428CCCCACCCCACCCCCCGCAC+6.72
SPI1MA0080.4chr12:57526738-57526752GACTTCCTCTTTCT-6.21
SPICMA0687.1chr12:57526738-57526752GACTTCCTCTTTCT-6.67
ZNF263MA0528.1chr12:57526746-57526767CTTTCTTCTTCCCCCTCCACT-6.32
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00100chr12:57519878-57554240Adipose_Nuclei
SE_01991chr12:57520288-57527431Aorta
SE_01991chr12:57527432-57528492Aorta
SE_04195chr12:57522419-57530997Brain_Anterior_Caudate
SE_05741chr12:57520316-57528205Brain_Cingulate_Gyrus
SE_06171chr12:57520260-57534210Brain_Hippocampus_Middle
SE_07493chr12:57520887-57533823Brain_Hippocampus_Middle_150
SE_07952chr12:57522404-57531077Brain_Inferior_Temporal_Lobe
SE_26173chr12:57522851-57530891Duodenum_Smooth_Muscle
SE_26822chr12:57525442-57528474Esophagus
SE_28331chr12:57526015-57527317Fetal_Intestine
SE_30586chr12:57525262-57528366Fetal_Muscle
SE_39018chr12:57520767-57527336IMR90
SE_44332chr12:57522407-57528487NHDF-Ad
SE_45184chr12:57525333-57528483NHLF
SE_46164chr12:57522434-57531208Osteoblasts
SE_46749chr12:57526044-57526519Ovary
SE_46749chr12:57526576-57527375Ovary
SE_46749chr12:57527459-57528226Ovary
SE_49434chr12:57522392-57528504Right_Atrium
SE_50286chr12:57520201-57528600Sigmoid_Colon
SE_52937chr12:57525285-57527386Small_Intestine
SE_52937chr12:57527412-57528434Small_Intestine
SE_55833chr12:57520023-57528498u87
SE_67616chr12:57520023-57528498u87
SE_68957chr12:57526846-57528260H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 7             
ChromosomeStartEnd
chr125752658657527444
chr125752813057528213
chr125752621257526408
chr125752660057527000
chr125752700057527302
chr125752780057528275
chr125752579957526525
Enhancer Sequence
TCTCTCTCCT CTCTTCATTT TCTCAACCAC CCTTCCACCA CTGAGCCTCC CAAAGGATGA 60
CAGCCCAGGT CCTGGCCAGA GTCAGTTCCT GTCCAGATGC CCCCATTCTT CAAAACCCCT 120
TCCTTACCTT TTGGGAAGCC CTTCCTTACT CAAGTCTATC TCTCTTTCCT CCTGCTGCAG 180
TGTGAGCCCT TGCACATCAG AACCCCCAAG CCTAGGTTTA TTCCCGCCCA GTACTCTCTT 240
CTCAGGGTCC TCCTCACTCC TCAGACTCTT TACCTTTCAG GTCCTCCAGC TCTGCGTGTG 300
GGCTCATTGC TCTTGGGGCA TCTGGGTGCA GCTGAATGGT ACTGCAGGAA GGCCCCTGAC 360
TTGGTAGTGC TGGGTATGAG CGATAGAGAA CCTGCCTCCC TCTTCTGTCC CAGATTTCAG 420
CCTGGTTAGC AGGATCCTGC ATTGTTTGGA GAAGGAAGCA GTTGGCTTTG GAGTGTTTCC 480
GGTGCAATGG CCTCAGGCAC CAATATAAAC CCTCCCTGGG AAAGAGGTGA GGGGTATATG 540
TGGAGAGTTG TCCCTCTTGC TCCCCTAGGG GAGATGAAAG CCTCTCCCTC TCCCACCAGG 600
CCTTAGCTTC CCTGGCTGAA GAGCTCCATT TTCCTCCCTC CTTTCTACCC TCCTGACTCC 660
AGGGGTGGTA GTGGTCCCTA TTCTGGGTCT CCCTTGAGTC AGGCACTGCC TAGGGCCGAG 720
ACTCTGTCTC TCCAAGATAG GACAGATCTT GCTCCCACCC TACTCTAGGC TCAGCGGGGT 780
AGTCATTCTC TGGGTTCATC CCAGGACAAC TGTGTCATCC CCTTGGCAAT CTCTGGACTG 840
AGCCCCCTTC CTGGCTTTTC TGGCTGTCTG TCTGTCTTTC TGTCTGTCTG TCATTAGTGT 900
GCGCTGTCTT GGCTTTTTAG AACCTCTCTG TCTCTCACCC TCTCAGTTCA TCTCTTACTG 960
CCGAACCTTT GTGACATTCT CTGCCCTGCT TTCTGCGTCT CTGTCACTTG TCTTATTTTT 1020
CTCTGCCTGT CTCCATTTAC CCCCATCCAG GCCTCTTGGT ATCCCAAAAG CTTCTTGGGA 1080
GCAAGAGTCT CTCTGGGCTT TCCCACTCAC CCCCTGGCTC CCTCCCCTCT GTTTTGGCTA 1140
TTTTTCCCCC TTCCTGGCCA GACCCAGTGT CCAGTTCAGC ACCAAAAGTT TCCTCTCCAC 1200
TTTCCTCCGA CTTCCTCTTT CTTCTTCCCC CTCCACTAAT TTGGGGAATG GGTTTTGGAG 1260
AGAATGTTTC TGGAAGAAAG GAACTTGATA CCCTTTGTGG GCTAAGAGGG AGAAAGGAGG 1320
TATTTCAGAA GGAAGGAGGG AGGTTAGACT TCTGGCAGAA CTTCCTCCTG ACCAGGAGCC 1380
TAAGAACTGG AGAAAGATGT AAGGAGTGAG TCAAGAACTT GGAGCTTTTA CTCTGGTGAG 1440
CATAAGCTGT GTGTGTGGCT GGGGTGGGGG GAGAAGGAGA GGAGGCTTAG AAATGCCTGG 1500
TGAGTGATAT GGTGACCTCT GGAGGCCTTC TGGGGGTCTG GCTTTTATTT GTGGGGAAAG 1560
GAAAAGCTGG TGGGGGAGGT CACGGGTCAG GCTAATGTCC TGCTGCATCA ATATTGACTC 1620
AGAATGGAAG CGGAGACCCT TCCCCTCCCC TGGCTGTCCA AGCCACCCTG TCTGTCTGTC 1680
TGTCCAGGCC GCAAAGCAGA GGCCCAGACT CAGGAATGAC AAAAATGTGT CTGAGCCTCA 1740
GGAAAGAGCC ACTGGGCAAC ACCCAAAATA CAAAAAATTC AGTGAAAACC TCTCGGTTTG 1800
GGTTTGGGAG GCCCTTGCTG CCCCACCCCC ATAAGGTCGA AAATTCAGAT TCCTGCAGGC 1860
TCTGTCCCCG CGCCGCCCCC CCACCCCACC CCCCGCACCT TGAGCATCCT CCTCCCACTC 1920
TGTTCCCTTA GCTATATCAT GTGGTTCCCT TTAGAGAACC CCCCTCTCAC CTAGCTCAGA 1980
GGGGAGCCTA TCTCTCCTTC TGCTGTGTCC ACTCTTAAAA AGGGCCCCAA GAGTCCCTGT 2040
CATGCTTTTG CAGTCCCTGA GTCTCCTTGT CCTTTAAGAA GCACCTCTAA GGTCTTAGCT 2100
CTCTTCCTTG CTCTCGCTCC CTCAAGGGGG TATCAAAGGA TGGGTTCCCC TCCTCTGGAG 2160
AAGACTCCTT CAGGGTTGGA CTTCGCTGTC ACCCTCTCTG GCCAGGCATT CTCACCCCAC 2220
TTCCCCACCC CCAAGGTCCC AGAATGGGAC ACAGAATGAC AGCCAAGGGT CAAGCAGGGC 2280
AGTGGGGTCT GTGTTGTGTC TGGACGCACA CCCAACTCTA CACCTCCTGC CCTGGCTCCA 2340
GCTTGGTGGC CCTGGGGACC GTGGCTGGGC TGGGTGCCTG GGTTTGGGGG GGTGGGGCAG 2400
GGTGTTGGCC AAGTTAGCAT GGCAGTCACA TTCATCTTCA GGCAAAGCCG AGAACAGACG 2460
GCCCCTGTGT CCTGGTGTTC TTCCTCCAAA CTCGCTCTCT CTCCTTCCTC TCTAGATCTC 2520
TCCTTCTTCT TCTCCTGCCT GTCTTCCCCT TCTTCTGTCC CATTCTTGCT CCTCTCTGTC 2580
TCCCCTATGC CCTTCCCTCC TCTCTGAGGA GCCCTGAAGG CCACCCCTTA AAATCCTCTC 2640
CCCACTGCCA GGGCCAGAGA ACGACAGCGT TCTCCCTGCA ATTTCCCTTC CTTGTTTTTT 2700
GTTTTTGTTT TGTTTTGTTT TTGAGACACA GTCTCACTCC ATCACCCAGA CTGAAATGCA 2760
ATGGCGTGAT CTCTGCTCAC TGCGACCTCC GCCTCCTGCT AATTTTTGTA TTTTTAGTAG 2820