EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS003-25405 
Organism
Homo sapiens 
Tissue/cell
A549 
Coordinate
chr2:43357230-43359500 
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: 1             
ChromosomeStartEnd
chr24335788943358928
Number: 1             
IDChromosomeStartEnd
GH02I043126chr24335394143368590
Enhancer Sequence
ACCTCTTTCC CCAGCCTCTG GCAGTGCCAT TGGAGGAACC GTCCCCTGAG GGTCATAGAG 60
GAAGCTGTCT GGCAGCTCAG AGGGTTGCCT CTTGTCCCTG CCCAGCCCCA CCGGCTTCCC 120
CTGGCTGCCT CCCTCACATG CCAGGCTTGG GCAGCTTCCC ATCACAGACC GAGGTCCAGC 180
CAGAGAGGCC TGTGCTCAGC CCCTCCCTGG GGCCTCTCAG TCTCCCCTCT CTGCTGTCCC 240
GCTCAAATGG TGGGGAGGGG GTAGAGTAGG ACAATTCAGA GAGAGGAACT AATCCCCTCC 300
CTCATCCCAC TGGGATGCAG AGGAGGAGGC CAGGCTGAAA GGGAACCACA CACATCTCCA 360
GTCACTTCTG TCATTGCTAT ACTGACCCTA CAGCACTTCC CATGTGCCAC TGGGCCTGCA 420
GGTCGGTATT GGCAAGGGTG AAGGTGAGGG GACGCAAAAG GGAATGCTAG GCTGTGGCGG 480
GGAAGGGCTG GCCTGGGCTC CCAGGAGGTG AGGGGCTGAG TCCCAGGTCA TGGTGGCCGG 540
ACACAGAGGC GGGTAGAAGG CCAGCAGGGC TGCCCCATCT GAGCCTGGGA GAGCCTGGGA 600
ACCCAAAGGC CCATCACAGA GGCTCGGAGG CAGCTGTGTC CACGCGAGAC AGAACTTAGG 660
CTGGACTTGG GGGTACAACC CCAGGATAAA CTTGGACACA TTGAAGGGCA AGCAGCTTGG 720
CCTCTGTCCA ACAGGAAACC CCCTCTGCAC AAGGAGAGAG GGAATGAGCA CAGAGTAGAG 780
GTGCCATGTG TTTCCCAGGG CTTCACTGCA GACAGCATCT CCTGGGAGGT AAACTGAGGC 840
CCCTGTGTGC AAAGCAAGAA ACTAGGGCAA GCCCCTTGGG GCTAAAGGTC AAGGAACTGA 900
AGGTTCCAAT TTACCTGCCC TGGTAGTTTC TGGCAAGAGA CCTCCACCGC CTTCCCTTCC 960
AGGATATGCC AGGCTGCAGG CTACAGTGCC GAGAAGGAGA AGACGGAGGC GGTGGTGATG 1020
TCACCCAAGG AATTAAGTAA GCAGGGGAGC TGATAACATC GTCCAGCCAG GCTCACTGTG 1080
GGCAGGGTGA CTCACTGAAG ACGGCCTGCG ATCGCCAGGT GATTGTTGTT GTGCCCAGCC 1140
TGTGGGGCTG GGGAGGAGGA AGGGGGGCAG GCCACAGAGC TGTGACAAGT TCCTCACCGA 1200
GGCCCCTGCT CAGGGGAGAG ACCTCAGTAC ACAGTGTCCT CCACCTCTGA GCCCGGGGCT 1260
GGCTCAGGAA ACAGCCCCCC TCTGCCTGTG CGATTATCTT TGTCCACAGT GTTTGGTGTG 1320
TGTTTGTGGG GTGTGTCAGG TGATTTTCCT GCCCGAAGCC TGCTGGGTGC TCCAGGTACT 1380
AGCGATTGCT CACAGCAGAG CAGTAGCCCC CTCCCTGGTT GGACAACTGT CTGTGGAGAC 1440
AACACCGGAT GGCAAACTGC TAACCGCAAC CACGTGGCGT CCTTACAGAG GGAACAGCCT 1500
GTTCCTCCCG CTGAGGGCAC CTGCAGACCT GCCCCATTCA TGGCTCCCTT CTCCCTCAGT 1560
CCCTGCTGAG GGGATGGTCC CTTCCCACCC TTAAGGGCAC CATGGACTGT TGTCCAAGTT 1620
GAGAACTGTC CAACTGCAGG GGGCACCATT CACTTGGCAG TCTTCGTGCC AGATGCTATG 1680
GCTGTCCACA GTGGCCCTGC CCCTTCCCTT TTGTAAATTA CTTCTCAGTT CCCTCCTCCA 1740
CCAGAATTAT CACACCAAAC TTTCCCCCAT GTATGCTTGC TTCTTTATCA CCTGACACTC 1800
TCATTCATTC ATTCCACAAA AAAATTGTGG CGTTTGTGCA AGGTACTATT CTAGGCAAGG 1860
GAACAAGACA GACCCTCCTG GAGCTCATGG AGTTCATATT CTAGCATGGG GGAGAACCAA 1920
TAAATAAATA ATTGGATACA TAAAACTGCA AGTGACAATA AGTGCTACAA AGAAAACTAA 1980
AGCCAGCCCA GGATAGAGGG TGATAGTGCC CTACTTCAGC TAGGACTGCC AGAAAGGCTT 2040
CTCTGTGGGG AGGTGGCCTC TGAGGGGAGA CCTGGAGGCA GCAAAGGAGG AAGCCTTCCC 2100
GGCAGAGCCC CTCCCATTGG CACCCAATGC CAAAAGAAGT TTCTATAACC CGTCCTGGTT 2160
CTGCCAGGAG CCTGCGGCAT GGCCTGGGGC GCTCAATTCC CAGTGCAGGG TGTCTATTTC 2220
TTCCCCCAAC AAACAAGAGG CCTAGTCGCA TAGTCTCTTC CAGCACAAAT 2270