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

TagContent
EnhancerAtlas ID
HS139-28593 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr2:43356790-43359520 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12466022chr243359061hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArMA0007.3chr2:43358719-43358736GGGAACAGCCTGTTCCT+6.41
ArMA0007.3chr2:43358719-43358736GGGAACAGCCTGTTCCT-6.55
NR3C1MA0113.3chr2:43358454-43358471CAGTACACAGTGTCCTC+6.16
NR3C1MA0113.3chr2:43358454-43358471CAGTACACAGTGTCCTC-6.1
NR3C2MA0727.1chr2:43358454-43358471CAGTACACAGTGTCCTC-6.17
NR3C2MA0727.1chr2:43358454-43358471CAGTACACAGTGTCCTC+6.28
PPARGMA0066.1chr2:43359225-43359245GAGGGTGATAGTGCCCTACT+6.06
PPARGMA0066.1chr2:43359224-43359244AGAGGGTGATAGTGCCCTAC-6.25
ZNF263MA0528.1chr2:43358378-43358399TGGGGAGGAGGAAGGGGGGCA+6.16
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_09287chr2:43352881-43363672CD14
SE_12072chr2:43356360-43368129CD3
SE_12638chr2:43357596-43357949CD34_adult
SE_12638chr2:43357983-43358394CD34_adult
SE_12638chr2:43359206-43359756CD34_adult
SE_15782chr2:43356249-43366275CD4_Memory_Primary_8pool
SE_16060chr2:43356269-43367833CD4_Naive_Primary_7pool
SE_16470chr2:43356387-43367955CD4_Naive_Primary_8pool
SE_17323chr2:43354132-43368330CD4p_CD25-_CD45RAp_Naive
SE_18231chr2:43354211-43368298CD4p_CD25-_CD45ROp_Memory
SE_20196chr2:43354257-43368691CD56
SE_21379chr2:43356282-43367987CD8_Memory_7pool
SE_21639chr2:43356455-43366302CD8_Naive_7pool
SE_21990chr2:43354317-43368146CD8_Naive_8pool
SE_22349chr2:43354363-43368357CD8_primiary
SE_23059chr2:43357256-43361322Colon_Crypt_1
SE_23724chr2:43357116-43362029Colon_Crypt_2
SE_24685chr2:43356376-43362104Colon_Crypt_3
SE_25333chr2:43347761-43368294DND41
SE_29578chr2:43357136-43358040Fetal_Muscle
SE_30898chr2:43356265-43368055Fetal_Thymus
SE_50400chr2:43354136-43362310Sigmoid_Colon
SE_52582chr2:43354327-43362297Small_Intestine
SE_53668chr2:43354129-43362161Spleen
SE_55101chr2:43356225-43362263Thymus
SE_58412chr2:43352450-43425007Ly1
SE_60594chr2:43354215-43369681DHL6
SE_61450chr2:43354337-43468354Toledo
SE_62203chr2:43354169-43468733Tonsil
SE_66770chr2:43357053-43359743Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr24335720043357800
chr24335788943358928
Number: 1             
IDChromosomeStartEnd
GH02I043126chr24335394143368590
Enhancer Sequence
AGTGAACACT TCCAAGAACC TTCATACTTA ATACCTCTAT CACTCCTCCA CTCAACAGGT 60
GAGGAAACAT CAGTCCAGTG AGAGTGGCAT GTGTGGGGAG GAGCCCAGGC TTGCTCTGAC 120
CTCTCTCTGG GGCCCCCCAC TCCAGAAGGT TGGAACAGCA TTCTACAGCA TTCCAGGATG 180
TGGAGGGGGC AGCAGTGTTT GTGTGCAGAG TGGCGAGGCC GACCTCCGAT GAGCTTCCCG 240
TAGGAAGGGT GCAGTGGGGG GTGCTCACCC TGCCCAGGGA TGCTATCTGC TCCAGGACTT 300
GTTTATCAGC CCACGGGGTG ATCGGCATGA CATCAATGGT GAGGTTTTTT GGGTTTCGTG 360
GTTTTGTTTT TTTCTTTTTC CTTCTAAGGA ACAATTCGTT TTGGTCAAAT AACTAGAGCA 420
AAAGTGACTG GTGTTTAGAC ACCTCTTTCC CCAGCCTCTG GCAGTGCCAT TGGAGGAACC 480
GTCCCCTGAG GGTCATAGAG GAAGCTGTCT GGCAGCTCAG AGGGTTGCCT CTTGTCCCTG 540
CCCAGCCCCA CCGGCTTCCC CTGGCTGCCT CCCTCACATG CCAGGCTTGG GCAGCTTCCC 600
ATCACAGACC GAGGTCCAGC CAGAGAGGCC TGTGCTCAGC CCCTCCCTGG GGCCTCTCAG 660
TCTCCCCTCT CTGCTGTCCC GCTCAAATGG TGGGGAGGGG GTAGAGTAGG ACAATTCAGA 720
GAGAGGAACT AATCCCCTCC CTCATCCCAC TGGGATGCAG AGGAGGAGGC CAGGCTGAAA 780
GGGAACCACA CACATCTCCA GTCACTTCTG TCATTGCTAT ACTGACCCTA CAGCACTTCC 840
CATGTGCCAC TGGGCCTGCA GGTCGGTATT GGCAAGGGTG AAGGTGAGGG GACGCAAAAG 900
GGAATGCTAG GCTGTGGCGG GGAAGGGCTG GCCTGGGCTC CCAGGAGGTG AGGGGCTGAG 960
TCCCAGGTCA TGGTGGCCGG ACACAGAGGC GGGTAGAAGG CCAGCAGGGC TGCCCCATCT 1020
GAGCCTGGGA GAGCCTGGGA ACCCAAAGGC CCATCACAGA GGCTCGGAGG CAGCTGTGTC 1080
CACGCGAGAC AGAACTTAGG CTGGACTTGG GGGTACAACC CCAGGATAAA CTTGGACACA 1140
TTGAAGGGCA AGCAGCTTGG CCTCTGTCCA ACAGGAAACC CCCTCTGCAC AAGGAGAGAG 1200
GGAATGAGCA CAGAGTAGAG GTGCCATGTG TTTCCCAGGG CTTCACTGCA GACAGCATCT 1260
CCTGGGAGGT AAACTGAGGC CCCTGTGTGC AAAGCAAGAA ACTAGGGCAA GCCCCTTGGG 1320
GCTAAAGGTC AAGGAACTGA AGGTTCCAAT TTACCTGCCC TGGTAGTTTC TGGCAAGAGA 1380
CCTCCACCGC CTTCCCTTCC AGGATATGCC AGGCTGCAGG CTACAGTGCC GAGAAGGAGA 1440
AGACGGAGGC GGTGGTGATG TCACCCAAGG AATTAAGTAA GCAGGGGAGC TGATAACATC 1500
GTCCAGCCAG GCTCACTGTG GGCAGGGTGA CTCACTGAAG ACGGCCTGCG ATCGCCAGGT 1560
GATTGTTGTT GTGCCCAGCC TGTGGGGCTG GGGAGGAGGA AGGGGGGCAG GCCACAGAGC 1620
TGTGACAAGT TCCTCACCGA GGCCCCTGCT CAGGGGAGAG ACCTCAGTAC ACAGTGTCCT 1680
CCACCTCTGA GCCCGGGGCT GGCTCAGGAA ACAGCCCCCC TCTGCCTGTG CGATTATCTT 1740
TGTCCACAGT GTTTGGTGTG TGTTTGTGGG GTGTGTCAGG TGATTTTCCT GCCCGAAGCC 1800
TGCTGGGTGC TCCAGGTACT AGCGATTGCT CACAGCAGAG CAGTAGCCCC CTCCCTGGTT 1860
GGACAACTGT CTGTGGAGAC AACACCGGAT GGCAAACTGC TAACCGCAAC CACGTGGCGT 1920
CCTTACAGAG GGAACAGCCT GTTCCTCCCG CTGAGGGCAC CTGCAGACCT GCCCCATTCA 1980
TGGCTCCCTT CTCCCTCAGT CCCTGCTGAG GGGATGGTCC CTTCCCACCC TTAAGGGCAC 2040
CATGGACTGT TGTCCAAGTT GAGAACTGTC CAACTGCAGG GGGCACCATT CACTTGGCAG 2100
TCTTCGTGCC AGATGCTATG GCTGTCCACA GTGGCCCTGC CCCTTCCCTT TTGTAAATTA 2160
CTTCTCAGTT CCCTCCTCCA CCAGAATTAT CACACCAAAC TTTCCCCCAT GTATGCTTGC 2220
TTCTTTATCA CCTGACACTC TCATTCATTC ATTCCACAAA AAAATTGTGG CGTTTGTGCA 2280
AGGTACTATT CTAGGCAAGG GAACAAGACA GACCCTCCTG GAGCTCATGG AGTTCATATT 2340
CTAGCATGGG GGAGAACCAA TAAATAAATA ATTGGATACA TAAAACTGCA AGTGACAATA 2400
AGTGCTACAA AGAAAACTAA AGCCAGCCCA GGATAGAGGG TGATAGTGCC CTACTTCAGC 2460
TAGGACTGCC AGAAAGGCTT CTCTGTGGGG AGGTGGCCTC TGAGGGGAGA CCTGGAGGCA 2520
GCAAAGGAGG AAGCCTTCCC GGCAGAGCCC CTCCCATTGG CACCCAATGC CAAAAGAAGT 2580
TTCTATAACC CGTCCTGGTT CTGCCAGGAG CCTGCGGCAT GGCCTGGGGC GCTCAATTCC 2640
CAGTGCAGGG TGTCTATTTC TTCCCCCAAC AAACAAGAGG CCTAGTCGCA TAGTCTCTTC 2700
CAGCACAAAT TCACCCACCT GTCGGCTTGA 2730