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

TagContent
EnhancerAtlas ID
HS026-07448 
Organism
Homo sapiens 
Tissue/cell
CNCC 
Coordinate
chr12:11917970-11920250 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3825083chr1211919407hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata1MA0035.3chr12:11920162-11920173TCCTTATCTCT+6.02
NFAT5MA0606.1chr12:11918421-11918431AATGGAAAAT-6.02
NFATC1MA0624.1chr12:11918421-11918431AATGGAAAAT-6.02
NFATC3MA0625.1chr12:11918421-11918431AATGGAAAAT-6.02
SOX10MA0442.2chr12:11919905-11919916TGCTTTGTTTT-6.02
ZNF263MA0528.1chr12:11919445-11919466TCTTCATGCTTCCCTTCCTCC-6.27
ZNF263MA0528.1chr12:11918994-11919015GAAGCAGGAGGAAGGTGTGGG+6
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_01754chr12:11918069-11920156Aorta
SE_09138chr12:11895682-11929433CD14
SE_12874chr12:11918556-11920257CD34_Primary_RO01480
SE_13315chr12:11914238-11920650CD34_Primary_RO01536
SE_14048chr12:11917909-11920987CD34_Primary_RO01549
SE_25354chr12:11914277-11930036DND41
SE_25772chr12:11913943-11922646Duodenum_Smooth_Muscle
SE_30380chr12:11917824-11920904Fetal_Muscle
SE_30906chr12:11914521-11920257Fetal_Thymus
SE_32458chr12:11910093-11922451GM12878
SE_39367chr12:11914420-11925956Jurkat
SE_43859chr12:11917454-11920221MM1S
SE_46110chr12:11915046-11920204Osteoblasts
SE_49833chr12:11914096-11919206RPMI-8402
SE_51622chr12:11918249-11920506Skeletal_Muscle
SE_54656chr12:11914202-11920959Stomach_Smooth_Muscle
SE_58379chr12:11878906-11990784Ly1
SE_58837chr12:11874923-11935776Ly3
SE_59849chr12:11874575-11943335Ly4
SE_61023chr12:11869475-11929777HBL1
SE_61926chr12:11879670-11927640Toledo
SE_62748chr12:11877030-11934459Tonsil
SE_66238chr12:11914420-11925956Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr121191879211919487
chr121191956611919967
Number: 1             
IDChromosomeStartEnd
GH12I011761chr121191442911925846
Enhancer Sequence
ATAGTGTTGA GTTCCCCTTT GAGATCTGAC TGTGGTTAAA GCTTCACAAA TTTCAGAAAA 60
ACAGAATAAC TCACTAAAAT AAAAATTTAA AGCTACCCCA CAGAAAACAT CTACCACAAC 120
CCAAAACTTC AGGGTTTATA TATCCAGATT TTAGTGAACT ATATGACTCT CCCTAGTCCC 180
TTGCTCTGTC TCCTGGTAAA TACTGTCCCT TTCAGAGCCC TGGCACATAC ATAGTGTAAT 240
AAGATCAGAC CCCATCCCCC TACCATTCCA ATGCAATCTA ATTGCAAAGT GAAAATCCAG 300
GGCCGTCTTA GATCCTCATC TGTCTACGTC TCTCTTGGTC CCCACTGCTT GATACGCAGT 360
CTCAGGTTCA ATACCATTCT CTCTTTTTGT GCTTTAGGTC TCTGTATTGT TTCCTTTTCA 420
CCACTTTTTT TTTTTTAATG AAGTGATTTT AAATGGAAAA TTAAAAACTT AACTGTGAAT 480
CTGGCAGTTT CCTGCTAATG CCTCTTTGCT AAGAAGCTTC ATAAAATACT GTATCTTATT 540
CACTTCAGCA CAGCTGCTGT GGGCTCTCAC CACTTAACCA TTCACAATAT GTCTGAGAGA 600
TTAATTTTTG TAAGGCTGTG GTTTGAGATA TCTCCCCCTT CCTTGTTTTA CTTAAAATCC 660
TCAGTGGGAA AGCGTGCATG GGGAAAAAAA AAACCACCAC CACCCTGGAT AAAAGGTACT 720
TTGGTAACAT ACGTGCTTTA GGAACTATAA TTTGTCATTT TATTTTCTTG TGCCCTCTTC 780
ATTTGAAATG CTGCAGCCTT TCTGCCAGAA GTCTCAAGTT TGTGTATGAG ACTGAGGGGG 840
AAACGAGAGT AGGTACCTTG TGCTGAGACT GTCCTGGGAC AGTCCCGTGG TGGGTGTGAG 900
CGTCTGTGTG ATGCAGGTAT GCTTATTTCT TCATGAAAGC CGCAGGTACT GGTTGCCTCT 960
CGCAGGGTTA AAACTCTTGG CGGCTCACAG GAGGTGATGA AGAGCAAGGG CACGGGAGAA 1020
TGAAGAAGCA GGAGGAAGGT GTGGGCCAGG GTCGGTTTCG GTGGGGTCCC CACTTGCTGG 1080
GTGAAAGCTG AACTGTTTAT CCACACATCC CAGCAGCAGC AGAAAGCCAA GGGGTGTTTT 1140
CAGGACTCAG CTGCCAAAGT TTCTTGAAGC AGCTCTGCTC AAAGGCATAT GCTGGGCTCA 1200
CTTCTGAGGG AAATTTCCTT TTTGGGGAAG TTGAAGCAAA GGAATTTCCT GTGTGGGCAG 1260
ACAGAGCTTC CTGACTTGAA GGCTTCTTGG AAGGGAAACA GTTTCATAAT GAAATGACAA 1320
ATTAAAGACA TACCAGCCGG GTTCACTTCA AAACAGCTAT TGAGAGTGCA GGCAAAGCCC 1380
TATTATACTC CCTCACAGAA CAAAAATAAA TCCCATCCTG ACAGGTTTCT GTATGCCGGA 1440
TTATATCCGT CCCCCCACAC CTTTCTTCAC AGCCTTCTTC ATGCTTCCCT TCCTCCCACC 1500
CCCGCCATTA GCTGCCACCA GCTCCATCTT GAACAGCTCT CGAGAGCAGC CGGCAGCCAG 1560
GCCGGGAGCC TGTTTCTTGC TCCCTTGCTT TGTGGCTTTG CCCATCCCTG ACCTGCGTGG 1620
AGGCCTTATA GGTTATGTGA CAGCCCTATG CTGCCAAGAC ACAGAAATGA CCTCTTTCCT 1680
TCCCCTTTTG ACATAAAGCA ATGATTGAAG ACGTCTTCAG CAATGGGGTG GGGGCGGGCA 1740
GTCAGGGGAG AATGCAGCCA TTTCCTCAGG CCGGCCTTTA AAATCTTGAA GGCAGTAAAT 1800
GTAAGTGCTA TTCCGGTCTT GGGAGCTGGG TCTGAATTCT TTGCTTTGTT GAAGGAAATA 1860
GGGCTCTGTG CTGGGTGGAC GATATTCTTG TACCTGAACA TGTCATTTTC TTCAGTTCCA 1920
TCAGCCTGCA TGTGGTGCTT TGTTTTGTTT CTGAAATTGA CATGATGATG CCTTAGGAAC 1980
TAAATTTTTT TCTTTAATGG AACAGGCTAG GAGAAAGAAG GATGGCGGTA TCATTTGGGG 2040
CGTGAGAACA GTCATTATTA ATTAGGCTTA AGTTAATGAA ATAAAAAAGG CACAGGCTTT 2100
GAAATCAGTT GTCTAAATTT AAGGGCCAGC TCTAACAATA TACAACCAGC AATGTAACCT 2160
TGAACAAGTC ACTGAACCTC CCAGCCTCAG TTTCCTTATC TCTAAAATGG GTACAGTCAT 2220
ACCTTTTTCA CATTGTTGTG AGGAAATTAG ATTATGATTT CAGAGGCACT TTGTGAATTC 2280