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

TagContent
EnhancerAtlas ID
HS098-46061 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr5:131804320-131806580 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2248116chr5131804347hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFE2L1MA0089.2chr5:131804529-131804544AAATGACTCATCAAT+6.39
PLAG1MA0163.1chr5:131806050-131806064CCCCAGTTGGCCCC-6.28
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00037chr5:131804384-131806816Adipose_Nuclei
SE_10915chr5:131798063-131818030CD20
SE_11856chr5:131806085-131811485CD3
SE_14495chr5:131804569-131805819CD4_Memory_Primary_7pool
SE_14495chr5:131805826-131811661CD4_Memory_Primary_7pool
SE_16304chr5:131806072-131807743CD4_Naive_Primary_8pool
SE_17370chr5:131798295-131804719CD4p_CD25-_CD45RAp_Naive
SE_17370chr5:131804876-131811594CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131804786-131818044CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131805804-131811428CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131805606-131808422CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131797758-131816289CD56
SE_20775chr5:131806027-131808256CD8_Memory_7pool
SE_21960chr5:131805342-131806664CD8_Naive_8pool
SE_22284chr5:131797996-131818026CD8_primiary
SE_25340chr5:131788298-131808279DND41
SE_27629chr5:131804613-131806872Fetal_Intestine
SE_28559chr5:131804285-131807800Fetal_Intestine_Large
SE_30917chr5:131804947-131805732Fetal_Thymus
SE_37771chr5:131804149-131807109HSMMtube
SE_39368chr5:131804343-131808265Jurkat
SE_42103chr5:131804676-131807088Lung
SE_50023chr5:131804207-131809752RPMI-8402
SE_50051chr5:131804590-131808491Sigmoid_Colon
SE_52336chr5:131804500-131808314Small_Intestine
SE_53285chr5:131804620-131808185Spleen
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_66244chr5:131804343-131808265Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 6             
ChromosomeStartEnd
chr5131804482131804534
chr5131805731131806058
chr5131805382131805709
chr5131805143131805318
chr5131806064131806314
chr5131806340131806486
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
GTAACCCAAG AGTCCCACTC CTCAGACTCT TCTCAAACCA CACTCTTACC CATGTGCACC 60
AGAATACCCA CACAGCACCA GAAAATGTCC AAATGACCAT CAAAAGTGGA GAGTACAAAT 120
AAATTGTGCA GTGTTCCTGG AGTGAAATGA ACTACAGCGA CTTGCAATAA CTGTAATATT 180
GTCATATTGG ATAATAATAC TGTAATAACA AATGACTCAT CAATGAATAA AACCTACAAA 240
AGAATGCATA CAGTATAATT CCTTTTAGCA AAAATTTAAC AGCTGGCAAA ACTGTATTGT 300
TAAGGATACA TGCAGAGGAG GTCAAACTAC AAAAAGCACA GAATTATTAC AAATGTCTAC 360
TTATGCAGAA GGGAGGGTTG GGGTTGTGAT TAGTAGGGGA ACACGTAGGT GCTTTGGGGG 420
TGCTAGTATT GTTTTCTCTC TTTAAGTTTG GGAGATTACC CTGGATTATT GGGTAGAAAC 480
TGGGGTGGGT GAGCCCAATG TAATCACAAG CATTCTTAAA TGGAGAAGAG AGAGGCAGAA 540
GGGTCAGAAG CAGAAGCAGA AGCAGAGAGA TTGCAATATA TGAAAGACCT GGCCAGCCAG 600
TGCTGGCTTT GAAGGTGGAG GAAGGGGCCG CAGGCCAAGG AATGCAGGCA GCCTCTAAAA 660
GCTGGAAAGG GGAAGAAAGG AAAGAGATTC TCTACTAGAG CCCCCAGGAA GGAATGCAGC 720
CCTGCTGACA CCTTCAGTTT AGCCCAGTGA GACCTGTTTT GGACTTCTGA CCTACGGAAC 780
TATAAGAAAA GAAATTTGTG TTGTTTTAAG CCCCTAAGTT TATGTTAGTT TATTAGAGCA 840
GCAACAGGAA GCTGATCCAC TGGGAAACCA TCTGGGATAT GCAGCTGCCC AAAATCCCTG 900
CTCGTGGTTA GATTCAGCCT TACGAGGCTC CACAGCCCCT CTGCGAAAGA CTCCATTCCC 960
TCTTGGAGAA GCTCAGACTC TAGAGCCCTG GGCAAGGAAT GGGCCTTCAT GGCATGGGGG 1020
CGATCAAGAA GGATGCCCCC CAGGACAGTG ACTCTGCTGG ACTTCTCTAC AGAAAACAGT 1080
ATATCCCTCA GTGGCATGAG AAGATCCAAT AGGGTCACCA CACTCCACAA CTGCAGGGGA 1140
CACTGTTCAC ATTTTAGTCT ATGCAGCCTC TGGTGGCCAA AGATTAAATG AGAACACCTT 1200
TGCTGTGTGA CCTGAAGTTC ATGGTCAGTA AATTGTAGCT ATTGTTATGC ACGACTTAGG 1260
GGGAAGCAGG GGTCACTGCA GAGCAGCAGT GGTTTTATAG AGATTTGCTT TATGATTATT 1320
TGTTAAACTG AACATATATT CTATGTATTT TTCTGCATAA TTATTGTTTC ACAATTTTTA 1380
AAAAGCATAT ACACACATGA ATCTTCTCTA GCCCCGAACA GCACAGTGAA TGGATAGGGC 1440
AGCAGATGAG CTCTGCCCCA CGCCGGCCCT GTTTCAGAAC AGCACTCCAG AGTGCCGCAC 1500
TGCTTGCTGA ACCACAGCTG TTACTGCAGA TTGAGGAGCC TCAGAGGGAA CAGAAGATAA 1560
AGATCATTAT GGAATTTAGG ATTGCAGGAC ATTCTTTGAC ATTTCATAAC AGCCAGGGGA 1620
GATCAACTGT GGTCAGGGGA CAGGGGCAGG AAGAAACCAT GGCCAAGGCC TGTCTGGCAG 1680
GACTTGAAGG GGCAGAGGGA CCCTTGCAAA TGACCCTGCC TGGAACCCAC CCCCAGTTGG 1740
CCCCTGTATA GCACTGATCC AGCTGGGGCT TTTATCCCAG GATACCCTCT TCAGGGATGC 1800
CTGTATTTGT TGATTATCTG CCATATGCCT GGTCACTGCA GAATACAAGG AAGAAAATAG 1860
CCTTCAGCAG AAGCTGAGAC AGGAGCCTAG AGGATGGACA GTAAGGAGTC GAAGGCTCAG 1920
GATGAGGCTT TCCTGACTTT CTCCCCTAGA GGACTGATGT TCTCTACTGG TACAGACCTT 1980
GTTTTATTCA TCCTTATGTC CCTAACCTGG AATGGGCCCA GGGTGACAGT TATAATAAGT 2040
GTTTGTCAAG TGAGCAAGTG TGTGGAGTGT GCATTGTAGA GAGTAAGGTC TCTACAGGAT 2100
CCTGCTGGAG AGGCAGCCCA CTGGGCTCAC CACTTCTCCA GAGGAGGGAC TGGTCCCTTG 2160
CCAGACAGCC CTGCCAGCTG GAGCAGGCTT CCTCAGGGGT GCCTGGAGCT GTTGACCATG 2220
GCTGTTGCCC TCTGGCCCCT CTTGGGAAGA GCAACCTGTC 2260