EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS053-32425 
Organism
Homo sapiens 
Tissue/cell
Foreskin_keratinocyte 
Coordinate
chr5:131780310-131783200 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1012793chr5131781345hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFKB1MA0105.4chr5:131781775-131781788TGGGGAATCCCCT+6.71
NFKB1MA0105.4chr5:131781775-131781788TGGGGAATCCCCT-6.82
PBX1MA0070.1chr5:131780367-131780379CCATCAATCAAT+6.62
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00037chr5:131779157-131783687Adipose_Nuclei
SE_01257chr5:131781288-131782044Adrenal_Gland
SE_01257chr5:131782565-131783056Adrenal_Gland
SE_02141chr5:131780861-131782049Aorta
SE_04124chr5:131781320-131782082Brain_Anterior_Caudate
SE_18258chr5:131780307-131784408CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131782266-131783478CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131782254-131783635CD56
SE_22284chr5:131780590-131783640CD8_primiary
SE_23079chr5:131782362-131783384Colon_Crypt_1
SE_23750chr5:131781511-131782081Colon_Crypt_2
SE_23750chr5:131782503-131783333Colon_Crypt_2
SE_25340chr5:131779182-131782135DND41
SE_25340chr5:131782161-131783524DND41
SE_25784chr5:131780866-131783705Duodenum_Smooth_Muscle
SE_26597chr5:131780491-131782132Esophagus
SE_26597chr5:131782434-131783530Esophagus
SE_30917chr5:131779275-131780673Fetal_Thymus
SE_30917chr5:131780689-131783539Fetal_Thymus
SE_31393chr5:131781154-131782071Gastric
SE_31393chr5:131782373-131783511Gastric
SE_39368chr5:131782618-131783324Jurkat
SE_40726chr5:131780478-131783608Left_Ventricle
SE_42103chr5:131780512-131782097Lung
SE_42103chr5:131782308-131783596Lung
SE_48659chr5:131780675-131782208Right_Atrium
SE_48659chr5:131782426-131783381Right_Atrium
SE_50051chr5:131780661-131782090Sigmoid_Colon
SE_50051chr5:131782357-131783496Sigmoid_Colon
SE_52336chr5:131780692-131782190Small_Intestine
SE_52336chr5:131782369-131783517Small_Intestine
SE_53285chr5:131780643-131782272Spleen
SE_53285chr5:131782375-131783378Spleen
SE_54554chr5:131781201-131782307Stomach_Smooth_Muscle
SE_55171chr5:131781262-131781723Thymus
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131781301-131782282Pancreatic_islets
SE_66244chr5:131782618-131783324Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr5131780800131782020
chr5131782323131782964
chr5131780608131782029
Number: 1             
IDChromosomeStartEnd
GH05I132443chr5131779344131783473
Enhancer Sequence
CATGTACCCA AAGTGGTCAG GCCACAATTT GGTTTTATAC ATTTTAGGGA GACATAGCCA 60
TCAATCAATG CATATAAGAT GTACATTGGT TCTGTCCAAA AAGGCAGGAC AACTAGGTTG 120
GGGAGTGGGG GTGGTTTCAA GTCATAGATG GATTCAAAAA TTTTTCTGAT TGACAATTGG 180
TTGAAAGAGT TATTATCAAT AGAAAGCAAC AGAAAGGAAT GTCTGGGTTA CGATAAGGGG 240
CTATGGGGAC CAAGGTTTTA TTATGCAGAT GAGGCCTCCA GGTAGCAGGC TTCAGAGAGA 300
ATGGACTGTA AATATCTCTT ATCAGTCTTA AAGAGTCAGT AATTCCAAAA GGGAAGAGGG 360
TATAACGAGG CATGTCTGGC TCCCCCTTCC CATCATGGCC TAAACTAGTT TTTCAGGTTA 420
ACTTTGGAAT GCCCTTGGCC GAGAGGAGGG GTCTATTCAG ACAGCTGGGG AGTACCTTGG 480
AATTTTCTTT TTGGTTTACA GAACACAGGC CCAGAAATGA GAACCAGGTT TAGGTCTTGC 540
TCTCCTACTC TCCACTGTGT GACTTGGGCA AGGCATCTAA TCTTTCTAAG CCTCAGTTTT 600
CTCATTTGTA GAATGGAAAT AATGCCCTTG CTTACTTCAT AGTGTCATTC AGAGGCACAG 660
ACGATAGAGA GGCAAAATTC TTGTCTTTAA CTGCCCTGAA GCTTCATGGA GGAGTTGGAC 720
AAGTACACAC ACAATGTGCT GCATACTACA CCAGAGGTAT GTCTAGGGTG TGGTAGTAGC 780
AGTGTGGAGG TAAACTAGTT CTGCCAAAAA GAGGAGACTA CAAAGCATGG GGCGTGGTGG 840
AAGTAGCCCT CCAGGGCTTT GGACTCTAAT GTTTCTCAAA CAGTAGAGTG TTAACTGTAT 900
TAAGTTGTAT TTAGTCCCTA CAACAAACCT GTGAGATAGG TGTCATCCAT TTCACATATG 960
AGCAGCTGAG GCTCAGAAAG GATCATGCAT TGGCCTGGCC TGGTATTTAT AGAGCCCCTG 1020
TTGAATGCTA AGGGGCGCAA ATCTAAGTTC CTTCCTCGTA GCTCACATTC CACAGGTGAA 1080
GTCACTTGCC CAAGACGAGG CTGGAATGTC AGAGCCTGGA TTCAAACCCT CATCTGGTGG 1140
CCTCCCACCT TACCCTAGAA CTCACTAGCC CTCAGGACAT CCTCTTACGG GGAGCATAGA 1200
CTGTCCCTGC CAGCCCCTGT GGGGAATTTG AGGATTTAGG GAAAAGGCTG GGTCAGGGAT 1260
AGGACAGGCC CTGCTACTCC TATGGAACCT TCTGTTTCCT GAGCATTCCC TGGCAGCCCC 1320
TCCCCAAAGA GAGATTGAAG GCCTGACCGT GCCAATGTTT TCCCCAGGGA CGGAGGGCAG 1380
GAGAAGCTTC CCCAGGGGAT TTCAAGGGAG GATGGAGGTG GTCTCTATTC TGGGGTCAGA 1440
GAGTGACACC CTCTTCCTGC TGAGGTGGGG AATCCCCTTG GATTTCTCTG GGTTTATGGG 1500
AGAGGCCTAT TGTTTTCGTA CTGATCAGGC CCTCAGGGGA GGAAAACTCA AGACCTGGCA 1560
TGTCATAGGA CTAAATCAGC CTCTGGCATC TGAGTGGCTC CTTAGGCTTG GGGCTCATTC 1620
CTGCCCTCCC ATGCCCTCAG CCTCAGGCTG CCATGAGACC CATGGCACTG CCACTGGGCA 1680
GTGACATTTT GTTTTAACCC AAGGAAATAA GAGATTGGCA AACCCCCTTC TCCAAGGAAA 1740
AATATACAGG ATTGTTTATT AGAGCATTTG CTGGTAGTAA CAATCATAGG AAACAATGTA 1800
AATGGCCAAT GTTTAGGAAT TAAATAAAAT ATGGTAAAAA TCTACATATA ATGAAATACT 1860
TTTAATGCAG CCATTTAAAC TCATTATGTA GAAGAAAATT AATTTCATGA GAAGAGTGCT 1920
TTATAACAGA TTTAGTCAAA ATTCAGATCA TAAAACACAA TGTACATGAT CTCATTTTTA 1980
ACCCAAGGAA ATAAGAAAAA AAATACCTAT ATATATGCAT AGAAGAATGT CTAGAAGGAT 2040
GCATCCAAAG TTAATTGTAG TTATTTCTGG GTAGTAGAAT GACACGTTTT CTCCTGTTTT 2100
CAATATTTCC AAGTTTCCTT CAGTGAAAAT GCATGTATTT TGTAATCATG GAGAAAAAGT 2160
TCCCATGGTG TGTATTGGCG AGAGAAGAGG ATTGTTTCCT TTTGGCTTTG CACTTAGATG 2220
GCCCAAGGCC TTGGCCTTGT TCCCAGAGTG CAGATATTGT AGAAGCCACG GGGAAGGCTG 2280
GGAGCAGCAG AGGAGAGGCC AGCTTGAGGA GAATAAGCTG GGCATCGCTG TCTAGGTGTC 2340
ATCCTAAATG TCACCTCCCA GAGAGGCACC TGACCACACA GCCTGGCGAA AGGAGGTCGC 2400
TCCCACACTT ACTCTGTGTG TTTCACCCCA GCTTACTGTC TTCATAGCAC CCATCTGCAT 2460
CTGAAGTTAC CTGCCTGCAT ATCCATTTCC TTGGTGATTA TTTATCTCCT GCACAGAAGG 2520
CAAGCTCTCC AAGAGCAGAG TCCCTTGCTC ACTCTGACTT CCCATTAGGA GAAAGGACCC 2580
AAGCCAGATC TTGGTCAACA AGCAACTGAG GACTTGCTCA GCAGCCCCAA GCTATGGGCA 2640
TTTATCCTAA GGCTACACAC AGCAGTGAGA AAAAGGAAAT AACTTCATAG GAATCTAGAA 2700
ACAGGTGGAG AGCTAGCTTA TAGGACCAGA CCTGGGTGGT GCTCAGCAAG CTGGAGGACC 2760
TGGCCCAGTG TTAGTAACAA CAGCGGCCAC GTACAGGTGT TGAGGAAGTA CCAGCTTTGT 2820
GTTTTCTCTT AAGGTGGAAC CAATGTAGGT TAGATCCCTC TCCCTCTGCT TCCAGCCCTC 2880
CTGCTGTCAC 2890