EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-46058 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr5:131796070-131797940 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs11745587chr5131796922hg19
rs6894249chr5131797547hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr5:131796318-131796336GCTTCCTGCCATCCTGCC-6.14
EWSR1-FLI1MA0149.1chr5:131796322-131796340CCTGCCATCCTGCCTTCC-6.76
POU2F2MA0507.1chr5:131797204-131797217AAATGCAAATGAA-6.59
ZNF263MA0528.1chr5:131797778-131797799GAAGGAGGAAGAACAGGGAGA+7.89
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00037chr5:131790656-131796338Adipose_Nuclei
SE_09163chr5:131788117-131797621CD14
SE_10915chr5:131787711-131797453CD20
SE_11856chr5:131788689-131797117CD3
SE_13479chr5:131790641-131796411CD34_Primary_RO01536
SE_14495chr5:131789106-131797177CD4_Memory_Primary_7pool
SE_17764chr5:131787920-131797394CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131787905-131797327CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131790791-131797009CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131788439-131797324CD56
SE_20775chr5:131790546-131796689CD8_Memory_7pool
SE_22284chr5:131788012-131797561CD8_primiary
SE_23079chr5:131794575-131796517Colon_Crypt_1
SE_23750chr5:131796561-131796935Colon_Crypt_2
SE_25340chr5:131788298-131808279DND41
SE_25784chr5:131790957-131797727Duodenum_Smooth_Muscle
SE_27629chr5:131790763-131801421Fetal_Intestine
SE_28559chr5:131794264-131804122Fetal_Intestine_Large
SE_30917chr5:131790670-131796844Fetal_Thymus
SE_31393chr5:131794548-131796995Gastric
SE_37771chr5:131791257-131796632HSMMtube
SE_39368chr5:131791092-131797698Jurkat
SE_40726chr5:131794433-131796690Left_Ventricle
SE_42103chr5:131794463-131796999Lung
SE_50023chr5:131791250-131797789RPMI-8402
SE_50051chr5:131790768-131797132Sigmoid_Colon
SE_52336chr5:131790812-131797015Small_Intestine
SE_52336chr5:131797662-131804003Small_Intestine
SE_53285chr5:131790524-131796944Spleen
SE_55171chr5:131794927-131796428Thymus
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_66244chr5:131791092-131797698Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr5131796798131796851
chr5131797501131797604
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
GAGAGTTCCC CATGCAGTGT GCTTCCCATT CTTACCAGCA GTTGGTATCT TCTGTCTTTT 60
TCACACTGGC CATCTGAGTC TCATAAGGAG ACTCCTCTCC TTCCACTGAG CCTGCATCCC 120
AGCCTCTCCC CTTTCTTCAG GGACCTCTCC CCAGCAATTA CGCCCTTCCA TTCTCTCAAC 180
CAGGGAATCT TCAAACTCTT CTTCTCCACT GGCTCCTGCT GTGCTCCTGT CTCCATCACC 240
TGTATAATGC TTCCTGCCAT CCTGCCTTCC CCGTGGAGTA CAGCCATGCT GTCTGCTGCT 300
TACAGCCAAG ATTCTGGAAA GAAATGTCTC CTTTTTCCTC GTCATCAACC ACTCATTTAT 360
TCAGCAAGTG TTTCTTTTAC ACTTGCCTGT GCTGGGCATG GCAGCAATGC AGCAGTGAAC 420
AAAACCATCA GCCCTGCTCT CATGCAGCTT ATAATCAAGT AGAGAGACAG ACATAAATGA 480
TTAATAGATG CTCCTGTAAT GGTGGTTGTG AGGTGTGCTG CCACAGCCCA GCCACACACG 540
CCAGTTCCCT TCTCTGCACA TGTACATGTC TGCTCATCCT TCCCACCTGA ACTCATGTGC 600
CACCTCACTT ATGCCCCTTC CCAATGCCGC ACCCACACAA CAGGGTGTCC CTCTGTGCCC 660
ACAGCAGCCC TTGGGTATAA CTGTTCCCCA CAGAGGCTGA ACCCCAAGGG CAGAGTCCAG 720
GCCACACTCA CCACGGAGAC CCCTGCCTGG CACAGAGCCC AGCCCAGCAG AGATGCTCAG 780
AAGATGAATG AAAGTCCCTG CTGAGATTGA TCCAATCTGT TTGTGAACAT CTCTGGGGTC 840
CAAGAATTCA CGGCTTTCTT TTTCTTTAGA GAGCCTTTTG TTTCTTTTTG CCATTATATA 900
CTATATTTGG GTTAGGGCAC AACAATGTGA ATATACTTAA TACTGAACTC TACACTTGAA 960
AATGGTTAAG ATGGTAAAGT TTTAAGTTAT ATGTATTTTG CCACAATTTT TTAAAATGCA 1020
GAGCATAGGT ACAAAGAAGG AAAAAAAGGG GGCAAGGTCC ATTTTATTGA GAAATAAAGA 1080
ACAAAGGGTT CAATTCAGAG AGGATTGGAT TTTAAAACGT AATTTAGATT AGGGAAATGC 1140
AAATGAAAAC CATAATAAGT AAGATACCAC TTCACATCTG TTAGGATGGC TATTTTAAAA 1200
CAACAAAAAC AACCTGAAAA TAAGTGTTGG CAAGGATGTG AAGAAATAGA TACCCTTGTG 1260
CATTGCTATT GGGAACGTAA AATCATGCAG CCTTTGTTGA AAACAATGTG GTGGTTCCTC 1320
AAAAACTTAG TTATCATATG ATCCCGCAGT TCCACTTCTA GGAATATACC CAAAAGAATT 1380
GAAAGCAGGG ACTCAAAGTG ATATTTGTAC ACCAGTGTTT GTAGCAGTAT TATTCACAAT 1440
AGCCAAAAGG TGGAAACAAC CCAGATGTCC ATGACAAGAG GAGTGGATAA ACAAAATATG 1500
GTGAATATGT ACAATGGAAC ATAATTCAGC TTTAAAAAGG AATGAAATTC TGGTACATGT 1560
TATAACATAG ATGAACCTTA AAAACATTAT GCTAAGTGAA ATAAGCCAGA CACAGAAGGA 1620
AAAATACCAG ATGATCCCAC TTATATGAGG TACCTAGAAT AGTGAAATTC ATAGAGACAG 1680
AAAGTAGAAG GATGGTTGCC AGGGGCTGGA AGGAGGAAGA ACAGGGAGAT ACTGCTTAGT 1740
GGATGCAGAG TTTATGTTGA GGGTGATGAA AAAGTTCTGG AGATGGATGG TGGTGATGGC 1800
TGCACAACAG TGAGAATGTA CTTCATACTA TGGAACTCTG CACTTAAAAA TGGTTAAAAT 1860
GGATGTAGAC 1870