EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-43041 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr2:43356710-43359140 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12466022chr243359061hg19
TF binding sites/motifs
Number: 7             
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
ZNF263MA0528.1chr2:43358378-43358399TGGGGAGGAGGAAGGGGGGCA+6.16
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_09287chr2:43352881-43363672CD14
SE_12072chr2:43356360-43368129CD3
SE_12638chr2:43357596-43357949CD34_adult
SE_12638chr2:43357983-43358394CD34_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
TCATTGAGGT GGGATCTCTT CTCTGAAATG TTCCCTCTCC CCTTTCCCTT CTCTGCAGGG 60
CCCCAGCCTC TTGGCTGGCC AGTGAACACT TCCAAGAACC TTCATACTTA ATACCTCTAT 120
CACTCCTCCA CTCAACAGGT GAGGAAACAT CAGTCCAGTG AGAGTGGCAT GTGTGGGGAG 180
GAGCCCAGGC TTGCTCTGAC CTCTCTCTGG GGCCCCCCAC TCCAGAAGGT TGGAACAGCA 240
TTCTACAGCA TTCCAGGATG TGGAGGGGGC AGCAGTGTTT GTGTGCAGAG TGGCGAGGCC 300
GACCTCCGAT GAGCTTCCCG TAGGAAGGGT GCAGTGGGGG GTGCTCACCC TGCCCAGGGA 360
TGCTATCTGC TCCAGGACTT GTTTATCAGC CCACGGGGTG ATCGGCATGA CATCAATGGT 420
GAGGTTTTTT GGGTTTCGTG GTTTTGTTTT TTTCTTTTTC CTTCTAAGGA ACAATTCGTT 480
TTGGTCAAAT AACTAGAGCA AAAGTGACTG GTGTTTAGAC ACCTCTTTCC CCAGCCTCTG 540
GCAGTGCCAT TGGAGGAACC GTCCCCTGAG GGTCATAGAG GAAGCTGTCT GGCAGCTCAG 600
AGGGTTGCCT CTTGTCCCTG CCCAGCCCCA CCGGCTTCCC CTGGCTGCCT CCCTCACATG 660
CCAGGCTTGG GCAGCTTCCC ATCACAGACC GAGGTCCAGC CAGAGAGGCC TGTGCTCAGC 720
CCCTCCCTGG GGCCTCTCAG TCTCCCCTCT CTGCTGTCCC GCTCAAATGG TGGGGAGGGG 780
GTAGAGTAGG ACAATTCAGA GAGAGGAACT AATCCCCTCC CTCATCCCAC TGGGATGCAG 840
AGGAGGAGGC CAGGCTGAAA GGGAACCACA CACATCTCCA GTCACTTCTG TCATTGCTAT 900
ACTGACCCTA CAGCACTTCC CATGTGCCAC TGGGCCTGCA GGTCGGTATT GGCAAGGGTG 960
AAGGTGAGGG GACGCAAAAG GGAATGCTAG GCTGTGGCGG GGAAGGGCTG GCCTGGGCTC 1020
CCAGGAGGTG AGGGGCTGAG TCCCAGGTCA TGGTGGCCGG ACACAGAGGC GGGTAGAAGG 1080
CCAGCAGGGC TGCCCCATCT GAGCCTGGGA GAGCCTGGGA ACCCAAAGGC CCATCACAGA 1140
GGCTCGGAGG CAGCTGTGTC CACGCGAGAC AGAACTTAGG CTGGACTTGG GGGTACAACC 1200
CCAGGATAAA CTTGGACACA TTGAAGGGCA AGCAGCTTGG CCTCTGTCCA ACAGGAAACC 1260
CCCTCTGCAC AAGGAGAGAG GGAATGAGCA CAGAGTAGAG GTGCCATGTG TTTCCCAGGG 1320
CTTCACTGCA GACAGCATCT CCTGGGAGGT AAACTGAGGC CCCTGTGTGC AAAGCAAGAA 1380
ACTAGGGCAA GCCCCTTGGG GCTAAAGGTC AAGGAACTGA AGGTTCCAAT TTACCTGCCC 1440
TGGTAGTTTC TGGCAAGAGA CCTCCACCGC CTTCCCTTCC AGGATATGCC AGGCTGCAGG 1500
CTACAGTGCC GAGAAGGAGA AGACGGAGGC GGTGGTGATG TCACCCAAGG AATTAAGTAA 1560
GCAGGGGAGC TGATAACATC GTCCAGCCAG GCTCACTGTG GGCAGGGTGA CTCACTGAAG 1620
ACGGCCTGCG ATCGCCAGGT GATTGTTGTT GTGCCCAGCC TGTGGGGCTG GGGAGGAGGA 1680
AGGGGGGCAG GCCACAGAGC TGTGACAAGT TCCTCACCGA GGCCCCTGCT CAGGGGAGAG 1740
ACCTCAGTAC ACAGTGTCCT CCACCTCTGA GCCCGGGGCT GGCTCAGGAA ACAGCCCCCC 1800
TCTGCCTGTG CGATTATCTT TGTCCACAGT GTTTGGTGTG TGTTTGTGGG GTGTGTCAGG 1860
TGATTTTCCT GCCCGAAGCC TGCTGGGTGC TCCAGGTACT AGCGATTGCT CACAGCAGAG 1920
CAGTAGCCCC CTCCCTGGTT GGACAACTGT CTGTGGAGAC AACACCGGAT GGCAAACTGC 1980
TAACCGCAAC CACGTGGCGT CCTTACAGAG GGAACAGCCT GTTCCTCCCG CTGAGGGCAC 2040
CTGCAGACCT GCCCCATTCA TGGCTCCCTT CTCCCTCAGT CCCTGCTGAG GGGATGGTCC 2100
CTTCCCACCC TTAAGGGCAC CATGGACTGT TGTCCAAGTT GAGAACTGTC CAACTGCAGG 2160
GGGCACCATT CACTTGGCAG TCTTCGTGCC AGATGCTATG GCTGTCCACA GTGGCCCTGC 2220
CCCTTCCCTT TTGTAAATTA CTTCTCAGTT CCCTCCTCCA CCAGAATTAT CACACCAAAC 2280
TTTCCCCCAT GTATGCTTGC TTCTTTATCA CCTGACACTC TCATTCATTC ATTCCACAAA 2340
AAAATTGTGG CGTTTGTGCA AGGTACTATT CTAGGCAAGG GAACAAGACA GACCCTCCTG 2400
GAGCTCATGG AGTTCATATT CTAGCATGGG 2430