EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-46060 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr5:131801480-131803740 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs2522056chr5131801726hg19
rs17622517chr5131803537hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR1MA0112.3chr5:131802673-131802690AGGCTCACAGTGACCTT-6.07
ESR1MA0112.3chr5:131802673-131802690AGGCTCACAGTGACCTT+6.28
EsrraMA0592.2chr5:131801817-131801828ATGACCTTGAG-6.02
EsrrgMA0643.1chr5:131801817-131801827ATGACCTTGA-6.02
LBX2MA0699.1chr5:131803142-131803152GCCAATTAGC+6.02
SPI1MA0080.4chr5:131803547-131803561CACTTCCTCTTTCT-6.51
ZNF263MA0528.1chr5:131803551-131803572TCCTCTTTCTTGACCTCCTCC-6.55
Number of super-enhancer constituents: 45             
IDCoordinateTissue/cell
SE_00037chr5:131801669-131804171Adipose_Nuclei
SE_01257chr5:131801990-131803186Adrenal_Gland
SE_09163chr5:131799339-131804166CD14
SE_10340chr5:131801416-131804001CD19_Primary
SE_10915chr5:131798063-131818030CD20
SE_11856chr5:131798507-131804031CD3
SE_13479chr5:131798645-131803817CD34_Primary_RO01536
SE_14495chr5:131799289-131803905CD4_Memory_Primary_7pool
SE_15423chr5:131801470-131803698CD4_Memory_Primary_8pool
SE_16304chr5:131799078-131803878CD4_Naive_Primary_8pool
SE_16894chr5:131801586-131803325CD4p_CD225int_CD127p_Tmem
SE_17370chr5:131798295-131804719CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131798263-131803976CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131797949-131803992CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131799050-131803746CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131797758-131816289CD56
SE_20775chr5:131799136-131804086CD8_Memory_7pool
SE_21523chr5:131801353-131804093CD8_Naive_7pool
SE_21960chr5:131799223-131803779CD8_Naive_8pool
SE_22284chr5:131797996-131818026CD8_primiary
SE_23750chr5:131801530-131801831Colon_Crypt_2
SE_23750chr5:131802106-131802595Colon_Crypt_2
SE_23750chr5:131802611-131803049Colon_Crypt_2
SE_25340chr5:131788298-131808279DND41
SE_25784chr5:131798529-131803921Duodenum_Smooth_Muscle
SE_26597chr5:131801478-131803762Esophagus
SE_27629chr5:131801861-131803896Fetal_Intestine
SE_28559chr5:131794264-131804122Fetal_Intestine_Large
SE_30917chr5:131801446-131803985Fetal_Thymus
SE_31393chr5:131801508-131803785Gastric
SE_37771chr5:131798722-131803794HSMMtube
SE_39368chr5:131801472-131803972Jurkat
SE_40726chr5:131801506-131803006Left_Ventricle
SE_42103chr5:131801441-131803807Lung
SE_43869chr5:131798062-131804366MM1S
SE_48659chr5:131801638-131803058Right_Atrium
SE_50023chr5:131801484-131803967RPMI-8402
SE_50051chr5:131801459-131803972Sigmoid_Colon
SE_52336chr5:131797662-131804003Small_Intestine
SE_53285chr5:131797984-131804080Spleen
SE_55171chr5:131801470-131803793Thymus
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_66244chr5:131801472-131803972Jurkat
SE_67186chr5:131798062-131804366MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr5131801987131802854
chr5131803262131803600
chr5131802496131802987
chr5131801595131801732
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
TTGCTCAGGC TAGTCTCGAA CTCCCAACCT CAGGTGATCC ACCCACCTCA GCCTCCCAAA 60
GTGCTGGGAT TACAGGCATG AGCCACCGTG CCGGGCTGAC AGTGGTTTTT AAAGGGGGAG 120
GGCAGATGAA GGACGTTGGT GGACCATCCT CTGGGAGGAG ATGTGGACTG AGGAAGCAAC 180
GCTGACCTCA GGCCCCACAC CACCCTTTCA CCTCAGCCTC ACTTTCTCAT CAGTAAATGG 240
AACTCGTTCT TGTGTATGTG CCATGGAGGC AATGTAGCAG AAGAGAATAG GGCAGACTTT 300
GGAACTCAGC CATCTGGGAG AAAATCCTAG TTATGTGATG ACCTTGAGCC AATGACTGAA 360
TTTCTCTGTC TCATTTTCTC TTCTGTAAAA TGGGGACAAT TACAGTGAAT TCTGTGAATT 420
CATTCATGTC CCTGACACAT GGTGTGAGCT CAGTCATTAC CTTTGCGAGG GTTGCAAGGA 480
TGTAATGAGA TGGCAGATGT GAGCACAGCT CCCAGACCCG AAGGTGCTGT ATGAATGGGA 540
GGGAGCAGTG AGTGTTATTT GGGAAATATT GAAGACACAA CTTCCCTCCC ACATTTGTCT 600
GGGGTGGAGC AACAGTTTTA CTTATTTAAT GATAAGCTGG AAGATGCACC AAAGGGAGGT 660
GAAAAACTGA AACCGCCAAC CGTTTGAGCT CCAGGCTGCA CCGAAGCGGT GTGGCTGGTG 720
CAGATGGTGA GAGCCCCAGT GCCGGCCCAC TTCCTCCATG AGTGCCACAC GCCTTTCTCA 780
AGCTAGCCGG CTTCCCAAGG CTGCAGGAAG TGGGGCCAGG AACAGGCCCT CCGGCTGTGT 840
TGGGGGAGGC CTGGGCAGGG GTTGGCAGCT GCTGGGTGTG AACGGAAGTC TTGGAGGTCC 900
TTGAAGGTCC TGGGGCCGCC TGCACAGCAG CCCCTGCCCT CTCCCTGTCC AGGCCTGCCC 960
AGGACTAGCT TGTAGCAGAC TCTTCTTGTA GCCTAGGCTC TTGCCTCTTG CAGTAGTGAG 1020
CCATTGTACA AAAGACATCC AGCGGAGGGA GGCAGGCTGG AGAGGAGGAC AGCCGAATCT 1080
TTTCTCAAAG GAAATGCAGT TGTGGTTTTG AGACGTTCAT ATTTCACATC TGTGGTTGGC 1140
GTTTCCCAGG GTTCTCAGAG GTGAATGCAG GGTCAGCCCT GTGTCACCAA ATAAGGCTCA 1200
CAGTGACCTT AGCAACAAGC TTTGCTGCCC ATTGGCTGTC ACTGCTGCCG CCTGCCAATG 1260
CGGCCTCCTG AAGGCCAGCA CTGATGCTGA GCTGAAACTT CTGCATGTGC CAAGGTCCAG 1320
CTGCCTCTGT CAGAAATCAC CGTCCTTGGA AGCAGCCACA GATAGGTAGA GAGCTCCGGA 1380
CAAAGGTGGA CAAGGTCAGT GGGAGGACTG TCCAGGTGTC CATGTTTCAG AGTCCACCTG 1440
GCCAGCATTC CATTCTCACA TAGCACCAAA CCAGCACCTT GGTGGCCTGG TCCCAGCTTG 1500
CCAGGACAAC CCCCCATTCC ACCCTGTCAA CCTTGAACTC TATAATGGTC ATCATTTCAT 1560
AGCTCTGCTC ATTTTAGTTC CACTGGGTTC TCCCTTGTGC TTGGCACTTG ACTAAGCTCC 1620
TTCTACACAT TACATCTTTT ACCTCTCTCA ACAACCCTGT GAGCCAATTA GCCCCATTTT 1680
ACAGGTGCAG AAACTGACAC CAAAGGAAGT CAGTAATGGC CCAGGTGACT GCACCACTAG 1740
TAAGTGGGGA AGTCAGAATT TAAACCCAAT TTAAACAGAC CTAGATCCCA TGCTATTAAC 1800
CATTGCACTG TATTGACAGA CACTCAATGT CCGTGCAGCT CAGTGTCTTC ATTCTGTGAC 1860
ATGGGGATGA CAGTACCGTA CCTCACAGGG TTGGGGTGAG CATTGTGTGG AGTGACTTAT 1920
GTCCAGAAGC ACACCTTTGC ACCAGTGGCC TTGGCACCCC CAAGGCATGC TCCACAAACA 1980
GCTTGCACAT TCCTTTCTCA CAGCGTGTGC TGCTGAAACA TTGAGGTTTG TGGACCGGAC 2040
TTCTCTGTAG CCCTTGTATT TAGTTTTCAC TTCCTCTTTC TTGACCTCCT CCCACCCCCC 2100
ACCCAACTGC AAGGTAGGGA GGCTACTGAG GGGCCAGCCT GTGGATTCCA GAGGGCACAG 2160
GGCTATCTGG GATGGAGGGG ACAGGGTTCT GAAGACAGAA GGTGGGAAGG TCACACTGTA 2220
AGGGCAGACA TACCCCATTT CTTCTACCTA AACAACTGGG 2260