EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-22078 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr2:43356900-43359540 
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
TTGCTCTGAC CTCTCTCTGG GGCCCCCCAC TCCAGAAGGT TGGAACAGCA TTCTACAGCA 60
TTCCAGGATG TGGAGGGGGC AGCAGTGTTT GTGTGCAGAG TGGCGAGGCC GACCTCCGAT 120
GAGCTTCCCG TAGGAAGGGT GCAGTGGGGG GTGCTCACCC TGCCCAGGGA TGCTATCTGC 180
TCCAGGACTT GTTTATCAGC CCACGGGGTG ATCGGCATGA CATCAATGGT GAGGTTTTTT 240
GGGTTTCGTG GTTTTGTTTT TTTCTTTTTC CTTCTAAGGA ACAATTCGTT TTGGTCAAAT 300
AACTAGAGCA AAAGTGACTG GTGTTTAGAC ACCTCTTTCC CCAGCCTCTG GCAGTGCCAT 360
TGGAGGAACC GTCCCCTGAG GGTCATAGAG GAAGCTGTCT GGCAGCTCAG AGGGTTGCCT 420
CTTGTCCCTG CCCAGCCCCA CCGGCTTCCC CTGGCTGCCT CCCTCACATG CCAGGCTTGG 480
GCAGCTTCCC ATCACAGACC GAGGTCCAGC CAGAGAGGCC TGTGCTCAGC CCCTCCCTGG 540
GGCCTCTCAG TCTCCCCTCT CTGCTGTCCC GCTCAAATGG TGGGGAGGGG GTAGAGTAGG 600
ACAATTCAGA GAGAGGAACT AATCCCCTCC CTCATCCCAC TGGGATGCAG AGGAGGAGGC 660
CAGGCTGAAA GGGAACCACA CACATCTCCA GTCACTTCTG TCATTGCTAT ACTGACCCTA 720
CAGCACTTCC CATGTGCCAC TGGGCCTGCA GGTCGGTATT GGCAAGGGTG AAGGTGAGGG 780
GACGCAAAAG GGAATGCTAG GCTGTGGCGG GGAAGGGCTG GCCTGGGCTC CCAGGAGGTG 840
AGGGGCTGAG TCCCAGGTCA TGGTGGCCGG ACACAGAGGC GGGTAGAAGG CCAGCAGGGC 900
TGCCCCATCT GAGCCTGGGA GAGCCTGGGA ACCCAAAGGC CCATCACAGA GGCTCGGAGG 960
CAGCTGTGTC CACGCGAGAC AGAACTTAGG CTGGACTTGG GGGTACAACC CCAGGATAAA 1020
CTTGGACACA TTGAAGGGCA AGCAGCTTGG CCTCTGTCCA ACAGGAAACC CCCTCTGCAC 1080
AAGGAGAGAG GGAATGAGCA CAGAGTAGAG GTGCCATGTG TTTCCCAGGG CTTCACTGCA 1140
GACAGCATCT CCTGGGAGGT AAACTGAGGC CCCTGTGTGC AAAGCAAGAA ACTAGGGCAA 1200
GCCCCTTGGG GCTAAAGGTC AAGGAACTGA AGGTTCCAAT TTACCTGCCC TGGTAGTTTC 1260
TGGCAAGAGA CCTCCACCGC CTTCCCTTCC AGGATATGCC AGGCTGCAGG CTACAGTGCC 1320
GAGAAGGAGA AGACGGAGGC GGTGGTGATG TCACCCAAGG AATTAAGTAA GCAGGGGAGC 1380
TGATAACATC GTCCAGCCAG GCTCACTGTG GGCAGGGTGA CTCACTGAAG ACGGCCTGCG 1440
ATCGCCAGGT GATTGTTGTT GTGCCCAGCC TGTGGGGCTG GGGAGGAGGA AGGGGGGCAG 1500
GCCACAGAGC TGTGACAAGT TCCTCACCGA GGCCCCTGCT CAGGGGAGAG ACCTCAGTAC 1560
ACAGTGTCCT CCACCTCTGA GCCCGGGGCT GGCTCAGGAA ACAGCCCCCC TCTGCCTGTG 1620
CGATTATCTT TGTCCACAGT GTTTGGTGTG TGTTTGTGGG GTGTGTCAGG TGATTTTCCT 1680
GCCCGAAGCC TGCTGGGTGC TCCAGGTACT AGCGATTGCT CACAGCAGAG CAGTAGCCCC 1740
CTCCCTGGTT GGACAACTGT CTGTGGAGAC AACACCGGAT GGCAAACTGC TAACCGCAAC 1800
CACGTGGCGT CCTTACAGAG GGAACAGCCT GTTCCTCCCG CTGAGGGCAC CTGCAGACCT 1860
GCCCCATTCA TGGCTCCCTT CTCCCTCAGT CCCTGCTGAG GGGATGGTCC CTTCCCACCC 1920
TTAAGGGCAC CATGGACTGT TGTCCAAGTT GAGAACTGTC CAACTGCAGG GGGCACCATT 1980
CACTTGGCAG TCTTCGTGCC AGATGCTATG GCTGTCCACA GTGGCCCTGC CCCTTCCCTT 2040
TTGTAAATTA CTTCTCAGTT CCCTCCTCCA CCAGAATTAT CACACCAAAC TTTCCCCCAT 2100
GTATGCTTGC TTCTTTATCA CCTGACACTC TCATTCATTC ATTCCACAAA AAAATTGTGG 2160
CGTTTGTGCA AGGTACTATT CTAGGCAAGG GAACAAGACA GACCCTCCTG GAGCTCATGG 2220
AGTTCATATT CTAGCATGGG GGAGAACCAA TAAATAAATA ATTGGATACA TAAAACTGCA 2280
AGTGACAATA AGTGCTACAA AGAAAACTAA AGCCAGCCCA GGATAGAGGG TGATAGTGCC 2340
CTACTTCAGC TAGGACTGCC AGAAAGGCTT CTCTGTGGGG AGGTGGCCTC TGAGGGGAGA 2400
CCTGGAGGCA GCAAAGGAGG AAGCCTTCCC GGCAGAGCCC CTCCCATTGG CACCCAATGC 2460
CAAAAGAAGT TTCTATAACC CGTCCTGGTT CTGCCAGGAG CCTGCGGCAT GGCCTGGGGC 2520
GCTCAATTCC CAGTGCAGGG TGTCTATTTC TTCCCCCAAC AAACAAGAGG CCTAGTCGCA 2580
TAGTCTCTTC CAGCACAAAT TCACCCACCT GTCGGCTTGA GGAACATGAC AGGAATCTGG 2640