EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS118-15341 
Organism
Homo sapiens 
Tissue/cell
Liver 
Coordinate
chr5:131808790-131811350 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs140316257chr5131809758hg19
rs11741255chr5131811182hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr5:131810769-131810790GATGGAGGAGGGGGAAGGTAA+6.27
ZNF263MA0528.1chr5:131810303-131810324CCTTCTGCCTCCTCCTTCTTC-6.44
ZNF263MA0528.1chr5:131810772-131810793GGAGGAGGGGGAAGGTAAGGC+6.63
ZNF263MA0528.1chr5:131810766-131810787GGAGATGGAGGAGGGGGAAGG+6.65
Number of super-enhancer constituents: 54             
IDCoordinateTissue/cell
SE_00037chr5:131810090-131812540Adipose_Nuclei
SE_01257chr5:131810577-131811720Adrenal_Gland
SE_04124chr5:131810599-131811590Brain_Anterior_Caudate
SE_06435chr5:131810039-131812439Brain_Hippocampus_Middle
SE_10340chr5:131806848-131810089CD19_Primary
SE_10915chr5:131798063-131818030CD20
SE_11856chr5:131806085-131811485CD3
SE_14495chr5:131805826-131811661CD4_Memory_Primary_7pool
SE_15423chr5:131808051-131809980CD4_Memory_Primary_8pool
SE_16304chr5:131807811-131811139CD4_Naive_Primary_8pool
SE_16894chr5:131808240-131809775CD4p_CD225int_CD127p_Tmem
SE_17370chr5:131804876-131811594CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131804786-131818044CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131805804-131811428CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131808474-131809746CD4p_CD25-_Il17p_PMAstim_Th17
SE_19103chr5:131810146-131811550CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131797758-131816289CD56
SE_20775chr5:131808533-131810109CD8_Memory_7pool
SE_20775chr5:131810171-131811664CD8_Memory_7pool
SE_21523chr5:131808484-131809915CD8_Naive_7pool
SE_21960chr5:131806740-131810211CD8_Naive_8pool
SE_22284chr5:131797996-131818026CD8_primiary
SE_23079chr5:131810420-131815180Colon_Crypt_1
SE_23750chr5:131809279-131809583Colon_Crypt_2
SE_23750chr5:131810479-131811551Colon_Crypt_2
SE_25340chr5:131808656-131817904DND41
SE_25784chr5:131810212-131813275Duodenum_Smooth_Muscle
SE_26597chr5:131808888-131809775Esophagus
SE_26597chr5:131810388-131811474Esophagus
SE_27629chr5:131808629-131817861Fetal_Intestine
SE_28559chr5:131808476-131817875Fetal_Intestine_Large
SE_30917chr5:131808333-131809877Fetal_Thymus
SE_30917chr5:131809910-131811467Fetal_Thymus
SE_31393chr5:131810363-131811622Gastric
SE_39368chr5:131808831-131809875Jurkat
SE_39368chr5:131809998-131811728Jurkat
SE_40726chr5:131809980-131815612Left_Ventricle
SE_42103chr5:131808719-131809822Lung
SE_42103chr5:131809951-131815230Lung
SE_48659chr5:131810417-131814893Right_Atrium
SE_50023chr5:131804207-131809752RPMI-8402
SE_50023chr5:131810017-131811707RPMI-8402
SE_50051chr5:131808593-131816260Sigmoid_Colon
SE_52336chr5:131808690-131816220Small_Intestine
SE_53285chr5:131808591-131809897Spleen
SE_53285chr5:131809900-131816337Spleen
SE_54554chr5:131810068-131812535Stomach_Smooth_Muscle
SE_55171chr5:131808723-131809332Thymus
SE_55171chr5:131810920-131811233Thymus
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131810440-131811582Pancreatic_islets
SE_66244chr5:131808831-131809875Jurkat
SE_66244chr5:131809998-131811728Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr5131810095131810374
chr5131810202131811200
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
GCACATCCGG TGTGAGCTGC GGGGCGGTGG CAGTGGCTGG GTCCTTTTCT CCCCTGGCCA 60
GGCTACACCC TTCTGCCTGT GGGTAAGACA GAGTTTTGAA GCGTCTGTGC TCACCCTTTC 120
CTCCCTAACA CAGGATGCTG TGATCATTCA CCCTATCAAA AGGCATGTGG GGTTGTGATC 180
GTTACTGTTT GCATCTCAAG TTGTGCGGCA CAATGTTTTC TCGTGTGTTA TCTCACCTGA 240
GACTCACACA CCCTGTGAGA CAGATAAGAC AAATGATGTT ATACCCATTT TACAGATGAA 300
GAAACTGAGG CTACAAAAGA TCTAGTGGCT TATTTGAGGC CACATAGCTA GTAAGTGGCA 360
GAGTGGGGAC TTTTTGCAGA TCTGGCTGGC ATCCAGTAAC TATTTTTTTT CCTCTATACT 420
TTTTTTTCCA GTAGTCCTAG CTTTTCCAGA GCTAAACTGA GTCCCCTTAG TATTCCCTTA 480
GTAAGGCCAA GGACTGAGAG TGTTATGAGT ATTGTGGATG TGTGGAGGGG CCATGCAACT 540
CCTTCCTGGG AATCTTAAGC CAAGCCCTGT GGCCTCTGAC TAGCTGTCCT AGGTGGCCTG 600
ACCTCAGGCA AGCCCCTCCA TGACCACTCA GAGCCAGCAC CTCAGCTCAC TGAGGTTTGG 660
GGAGGGGGCT CAAAGAGGCA GCTGCTTCCT ATAGAGAGGT CCAGCAGAGG CACTATCCTG 720
GGGGGCATCC TTCTTGACCC CCTCCATGCC ATGGAGGCCC ATTCCCTGCC CAGGGCTTTA 780
GAGTCTGAGC TTCTCCCAGA GGGAATGGAG TCTTTCACAG AGAGGCTGTA GAGCCTTGTG 840
AGGCTGAGTC CAACCCACGT GCAGGGATTT TGGGCAGCTG CATCCCCCAA ATGGTTTCCC 900
AGTGGATCAG TTTCCTATTG CTGCTCTAAC AAATTATCAT AAACAGGGGC TTAAAACAAC 960
ACAATTTTTT ATTTATTTAT TTATTTTTTT GGATACAGGG TCTTGCTCTG TCACTCAGGC 1020
TGGAGTGCAG TGGCTCAATC TTGACTCACT GCAACCTCTC CCTCCTGGGC TCAGGCCATC 1080
CTCCTACCTC AGCCTCCCAA GTAGCCAGGA CTAAAGGCAC GTGCTACCAC ACCTGGCTAA 1140
TTTTTTGTAT ACTTTATAGA GACAGGGTCT CACTATGTTG CCCTGGCTGG TCTCAAACTC 1200
CTGGGCACAA GCAATCTGCC TGCCTCAGCC TCCCAAAGTG CTAGGATTAC AGGTGTAAGC 1260
CACTGCACCT GGCCCGTTTC TTTTCTTATA GTTCTGTAGT CAGAAGTCCA AAACAGGTCT 1320
CACTGGGCTA AACTCAAGGT GTCAACAGAG CTGCATTTCT TCCTGGGGGC TCTAGTGGAG 1380
AATCCCTTTC CTTCCTTTCC CTTTCCAGCT TTTAGAGGCT GCCTGCATTC CTTGGCCTGC 1440
AACCCCTTCC TCCACTTTCA AAGCCAGCAC TGGCTGGTCA GGTTTTTCAC AATGCGATCT 1500
CTCTGGTTCT GACCCTTCTG CCTCCTCCTT CTTCATTTAA GAACCCTTGT GATTACACTG 1560
GGCCCACACC AATAATCCAG GGTAATCTCT CTATTTGCAA GTGAGCTGGT TAGCAACCTT 1620
AATTCCATCT GCAGTTTTAA TTCCTCTTTG CCATGTAGCA ACATATTCAT AGGCTCATGC 1680
ATTAGGACGT GGACCTCTTT ATTCCACTGT GGACCAATAC TCTGCCTTCC ACACCTAGCC 1740
TCTCTTCTGA GTTTTCCAAG GGCCCCCCAT CCTCAGGCAT CCTCAGGCAT AGACAGCCGG 1800
CTGGGCCAGA CCACAGTCAG GATGTTCCCG CCACTATCAG AGAGGTCCTT TCTACCTAAG 1860
TCCCCTCCCA CCTGCCTGCT CCTCTTTCAG CTCGGTCTGT CCTGGATTCC TCTTCCTTCA 1920
TCCTCTGCTC CCAGTCTTAG GTAGAGAAGA GCTGAGCAGG AAGTGCCAGG GGGTGTGGAG 1980
ATGGAGGAGG GGGAAGGTAA GGCCTGAGGC ACCAGGGCTC TGGGAGCCCA GGGAGCTGAG 2040
GCCTTTCAAT CCAGACACCC TGCACTTCTC TGGCTCTGGG GCCTCTGGGG ACCACACACT 2100
CAGCTCCAGG GCTGGAGGGG TGGCCAGCCA AGTATTGGAA CCCTTCTGCT TGTACATCCC 2160
TAGCTGCCCT TAACAGCCAC AGTTCACCTG GCCCTTTTCT TGGGTGATGA CAGACTGTCT 2220
GCCTTAATTT ATTCCCTTTC CCCTGTCCCT CCCTAGGCCT CAGGCTGGAA CTTTCAGGAG 2280
CTTCCACGGG AGGCAAGGCC CCAGCCAGGC CTCTGTCCCT GGGCTGCTTG GTGTGGGGAT 2340
GGGGGATCCA GAACCCCAGC AGGAGGGCAG ATGGGGAGCA CAGGGCAGGA GGGGCAGGAC 2400
AAAGCCTTTG GCCCTCAGGG AGGGTGACCA ACTGGCCCTG GTTTGCCTGG GACTTTCCCA 2460
GTTTTAGCAC TGAAAGTCCC AAATCCTGGG AAACTCCTCA GTCCTAAGCA AACTGGAACA 2520
GTTGGTCAGC CTATCTCCAA GCCTTTTGCA CCTCCTAATC 2560