EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS046-29590 
Organism
Homo sapiens 
Tissue/cell
Fetal_muscle_leg 
Coordinate
chr5:131780650-131783150 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1012793chr5131781345hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFKB1MA0105.4chr5:131781775-131781788TGGGGAATCCCCT+6.71
NFKB1MA0105.4chr5:131781775-131781788TGGGGAATCCCCT-6.82
Number of super-enhancer constituents: 37             
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_30917chr5:131780689-131783539Fetal_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: 2             
ChromosomeStartEnd
chr5131780800131782020
chr5131782323131782964
Number: 1             
IDChromosomeStartEnd
GH05I132443chr5131779344131783473
Enhancer Sequence
AATTCCAAAA GGGAAGAGGG TATAACGAGG CATGTCTGGC TCCCCCTTCC CATCATGGCC 60
TAAACTAGTT TTTCAGGTTA ACTTTGGAAT GCCCTTGGCC GAGAGGAGGG GTCTATTCAG 120
ACAGCTGGGG AGTACCTTGG AATTTTCTTT TTGGTTTACA GAACACAGGC CCAGAAATGA 180
GAACCAGGTT TAGGTCTTGC TCTCCTACTC TCCACTGTGT GACTTGGGCA AGGCATCTAA 240
TCTTTCTAAG CCTCAGTTTT CTCATTTGTA GAATGGAAAT AATGCCCTTG CTTACTTCAT 300
AGTGTCATTC AGAGGCACAG ACGATAGAGA GGCAAAATTC TTGTCTTTAA CTGCCCTGAA 360
GCTTCATGGA GGAGTTGGAC AAGTACACAC ACAATGTGCT GCATACTACA CCAGAGGTAT 420
GTCTAGGGTG TGGTAGTAGC AGTGTGGAGG TAAACTAGTT CTGCCAAAAA GAGGAGACTA 480
CAAAGCATGG GGCGTGGTGG AAGTAGCCCT CCAGGGCTTT GGACTCTAAT GTTTCTCAAA 540
CAGTAGAGTG TTAACTGTAT TAAGTTGTAT TTAGTCCCTA CAACAAACCT GTGAGATAGG 600
TGTCATCCAT TTCACATATG AGCAGCTGAG GCTCAGAAAG GATCATGCAT TGGCCTGGCC 660
TGGTATTTAT AGAGCCCCTG TTGAATGCTA AGGGGCGCAA ATCTAAGTTC CTTCCTCGTA 720
GCTCACATTC CACAGGTGAA GTCACTTGCC CAAGACGAGG CTGGAATGTC AGAGCCTGGA 780
TTCAAACCCT CATCTGGTGG CCTCCCACCT TACCCTAGAA CTCACTAGCC CTCAGGACAT 840
CCTCTTACGG GGAGCATAGA CTGTCCCTGC CAGCCCCTGT GGGGAATTTG AGGATTTAGG 900
GAAAAGGCTG GGTCAGGGAT AGGACAGGCC CTGCTACTCC TATGGAACCT TCTGTTTCCT 960
GAGCATTCCC TGGCAGCCCC TCCCCAAAGA GAGATTGAAG GCCTGACCGT GCCAATGTTT 1020
TCCCCAGGGA CGGAGGGCAG GAGAAGCTTC CCCAGGGGAT TTCAAGGGAG GATGGAGGTG 1080
GTCTCTATTC TGGGGTCAGA GAGTGACACC CTCTTCCTGC TGAGGTGGGG AATCCCCTTG 1140
GATTTCTCTG GGTTTATGGG AGAGGCCTAT TGTTTTCGTA CTGATCAGGC CCTCAGGGGA 1200
GGAAAACTCA AGACCTGGCA TGTCATAGGA CTAAATCAGC CTCTGGCATC TGAGTGGCTC 1260
CTTAGGCTTG GGGCTCATTC CTGCCCTCCC ATGCCCTCAG CCTCAGGCTG CCATGAGACC 1320
CATGGCACTG CCACTGGGCA GTGACATTTT GTTTTAACCC AAGGAAATAA GAGATTGGCA 1380
AACCCCCTTC TCCAAGGAAA AATATACAGG ATTGTTTATT AGAGCATTTG CTGGTAGTAA 1440
CAATCATAGG AAACAATGTA AATGGCCAAT GTTTAGGAAT TAAATAAAAT ATGGTAAAAA 1500
TCTACATATA ATGAAATACT TTTAATGCAG CCATTTAAAC TCATTATGTA GAAGAAAATT 1560
AATTTCATGA GAAGAGTGCT TTATAACAGA TTTAGTCAAA ATTCAGATCA TAAAACACAA 1620
TGTACATGAT CTCATTTTTA ACCCAAGGAA ATAAGAAAAA AAATACCTAT ATATATGCAT 1680
AGAAGAATGT CTAGAAGGAT GCATCCAAAG TTAATTGTAG TTATTTCTGG GTAGTAGAAT 1740
GACACGTTTT CTCCTGTTTT CAATATTTCC AAGTTTCCTT CAGTGAAAAT GCATGTATTT 1800
TGTAATCATG GAGAAAAAGT TCCCATGGTG TGTATTGGCG AGAGAAGAGG ATTGTTTCCT 1860
TTTGGCTTTG CACTTAGATG GCCCAAGGCC TTGGCCTTGT TCCCAGAGTG CAGATATTGT 1920
AGAAGCCACG GGGAAGGCTG GGAGCAGCAG AGGAGAGGCC AGCTTGAGGA GAATAAGCTG 1980
GGCATCGCTG TCTAGGTGTC ATCCTAAATG TCACCTCCCA GAGAGGCACC TGACCACACA 2040
GCCTGGCGAA AGGAGGTCGC TCCCACACTT ACTCTGTGTG TTTCACCCCA GCTTACTGTC 2100
TTCATAGCAC CCATCTGCAT CTGAAGTTAC CTGCCTGCAT ATCCATTTCC TTGGTGATTA 2160
TTTATCTCCT GCACAGAAGG CAAGCTCTCC AAGAGCAGAG TCCCTTGCTC ACTCTGACTT 2220
CCCATTAGGA GAAAGGACCC AAGCCAGATC TTGGTCAACA AGCAACTGAG GACTTGCTCA 2280
GCAGCCCCAA GCTATGGGCA TTTATCCTAA GGCTACACAC AGCAGTGAGA AAAAGGAAAT 2340
AACTTCATAG GAATCTAGAA ACAGGTGGAG AGCTAGCTTA TAGGACCAGA CCTGGGTGGT 2400
GCTCAGCAAG CTGGAGGACC TGGCCCAGTG TTAGTAACAA CAGCGGCCAC GTACAGGTGT 2460
TGAGGAAGTA CCAGCTTTGT GTTTTCTCTT AAGGTGGAAC 2500