EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-46059 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr5:131799450-131801300 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3749833chr5131799626hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr5:131801275-131801287GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr5:131801279-131801291GTTTGTTTGTTT+6.32
IRF1MA0050.2chr5:131800086-131800107AACTGGAAAATGAAACTGGAA-6.52
IRF2MA0051.1chr5:131800090-131800108GGAAAATGAAACTGGAAA+6.32
TFAP2CMA0524.2chr5:131800036-131800048TGCCCTGAGGCA-6.18
ZNF263MA0528.1chr5:131800189-131800210GAAGCAGGAGTGGGAGTGGGG+6.05
Number of super-enhancer constituents: 48             
IDCoordinateTissue/cell
SE_00037chr5:131799090-131801306Adipose_Nuclei
SE_01257chr5:131800016-131800566Adrenal_Gland
SE_04124chr5:131799520-131800927Brain_Anterior_Caudate
SE_06435chr5:131798169-131800532Brain_Hippocampus_Middle
SE_09163chr5:131799339-131804166CD14
SE_10340chr5:131799360-131801262CD19_Primary
SE_10915chr5:131798063-131818030CD20
SE_11856chr5:131798507-131804031CD3
SE_13479chr5:131798645-131803817CD34_Primary_RO01536
SE_14495chr5:131799289-131803905CD4_Memory_Primary_7pool
SE_15423chr5:131799427-131801062CD4_Memory_Primary_8pool
SE_16304chr5:131799078-131803878CD4_Naive_Primary_8pool
SE_16894chr5:131799488-131801389CD4p_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_21523chr5:131799315-131801183CD8_Naive_7pool
SE_21960chr5:131799223-131803779CD8_Naive_8pool
SE_22284chr5:131797996-131818026CD8_primiary
SE_23079chr5:131798256-131801316Colon_Crypt_1
SE_23750chr5:131799600-131801308Colon_Crypt_2
SE_25340chr5:131788298-131808279DND41
SE_25784chr5:131798529-131803921Duodenum_Smooth_Muscle
SE_26597chr5:131799534-131801338Esophagus
SE_27629chr5:131790763-131801421Fetal_Intestine
SE_28559chr5:131794264-131804122Fetal_Intestine_Large
SE_30917chr5:131797969-131801440Fetal_Thymus
SE_31393chr5:131799442-131801362Gastric
SE_37771chr5:131798722-131803794HSMMtube
SE_39368chr5:131797788-131801346Jurkat
SE_40726chr5:131799515-131801300Left_Ventricle
SE_42103chr5:131798108-131801401Lung
SE_43869chr5:131798062-131804366MM1S
SE_48659chr5:131799596-131801154Right_Atrium
SE_50023chr5:131797791-131801335RPMI-8402
SE_50051chr5:131798009-131801379Sigmoid_Colon
SE_52336chr5:131797662-131804003Small_Intestine
SE_53285chr5:131797984-131804080Spleen
SE_54554chr5:131799233-131800545Stomach_Smooth_Muscle
SE_55171chr5:131799589-131801335Thymus
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131799231-131801494Pancreatic_islets
SE_66244chr5:131797788-131801346Jurkat
SE_67186chr5:131798062-131804366MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr5131800033131800450
chr5131800635131801220
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
TTGTCCTTAA ATCCTCTTGG ATTAGGCTAT AAATTGCAAA TAAATGGAGC AACAGACAGA 60
GCAAAAGCAC ATAAGGTCCT TTAATAGAAT TTCTCTATCT TATTCTGTTT CTATGAATGC 120
CTGTTACAAA TTAGCAGCTT AAAGGGAAAC CTGGAGTGTG GGAAAGAGCG ACCCTTGTGT 180
GAAGTCCACA GCCGGGGTTT CCTACAGACC TCAGGTCCCA GAGAACATCT AAGATGCCTC 240
CAACACCAGA TGGAGGAGGG CAGGAGATGC TGCACAGAGA AGCAGCACTT CCCGAGCATC 300
TGTGGCAGGA AGTGACTTGG AGAGGATGAG GCCGTGCCTC AGGTGTGCTC TAGCTGTTCT 360
GATGGTCTCT GAGGCCACGA CTGCCATGGT GAGGTCCACA GCCTGCATCA GAATCACCAA 420
AGGGCCCAAA CGTACGGCCT CAGAGCCTGG AGAGCCAGGA ATCGGCATTG CAACAACTCC 480
CTGCTCAGTG GGTTCTACCA GTCCAGTACC TGCCCTCTGA GGGTGCCCAG GGAGCAGGGT 540
GCTTGCTGGC TGGAACACTT TTTCCTGCCC CTCAGCTCCT CTGTGATGCC CTGAGGCACG 600
GGCACTGGAA AGCTGGCAGA GCTGCTTCTA AATTGAAACT GGAAAATGAA ACTGGAAATC 660
ACAGTTTCAT TTTCCAGTTT CACTCGCTCC CCCTACTGTT GGGGTTTCTT TTCCACAAGG 720
AGAGTCCCCC AGGGAGAAAG AAGCAGGAGT GGGAGTGGGG GAGCATGTTG GGGGAAGGCA 780
GTGAGGGTGT CCTGTCTGCA GCAGGGCATG GAGGGGCCCC AGCGCTGCAC TTGCTTCCTT 840
TAAGCCTGGC CTGCTTGCTG TCAGCCCCGG GGGTGGTTTC CTCTCTAGGA AAAGCTAATG 900
TCATGCTTAT GCTGAAAAAC TCTTTTCAGA GGTACTTTAG GAGGGGCCTG GCTCTCGATT 960
AATCTGGGCC ATTTCATACC GGCTGTGCTC ACCCAGGCAC AAACACTGAA AGCAACAGCT 1020
GGCAAAGCCA TCGCTTGGTA GCAGCTTGGA AGACACCACC AAAGAAGCTC TCATGGAAGC 1080
GGCAGATTTC CTGAAGCGAC TGGAATGCGG GGAAGGAGGG CAGTCGGGGA GAGCCGAGAA 1140
CCAGCCCCCC TGCCAACTCC ACCCCATTCC TCTCCTCACC TGAAATGTCT CATCCTTAGA 1200
ACAGCTGCCC TAACCCCCTA ATCCCACACA CTCCTTTGTA GGTTAAGACC CCTGAAGTTG 1260
CACCCTCTCG TAGGAGCTAT GTTTTTCAGA GATCCATGTG ATTATTTGCC TAATGTCTGC 1320
CTCCCTCAGG GAAGTAAAGT CTGTGACGCG TGGACCTGGT CTGTGTTGTT CACTGTGCAT 1380
CCACAGTGCC TGGGTAGTGC CTGGCATGCA GGAAGTACAC ACAAAAAATA TGTGTTCATG 1440
AGTGAGGGCA GGCTTGAAGA GCCCAAGAGA AGGACAGTGC TCCAGGGAGG CGTCTGCATC 1500
AGGCTCCCCA GTGTCTGGAC TGCATCCCAG CCCCTCCGAG CAACTTCAGG GGAGGATTCT 1560
GTGAACAGAT GCCCCAGCTC TTCCGCCCAC AGCTCCTACC CCCAGCCTGA GGAATGCTTT 1620
GACTGTCCCC AGTGTGTGCA GGCAGTGGGG AGGTGATAGG GGGAGGTGTC CCACATGGCA 1680
CACTCTCCCT AGCCCTTGCT TTGCCTCCGT TACCTACATA GATGGGCTTC ACAGCCTCTT 1740
CCAGATAGGC AGGGCACTGA GCTCTGTGGG CCACACCTAA AAAGAAAGGG AGACAAGCTG 1800
GCGGTGGGGG CATGACAGTG TTTTTGTTTG TTTGTTTGTT TTTTGAGATG 1850