EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-69109 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr6:43742120-43745200 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs833070chr643742626hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr6:43742693-43742704GCCCCGCCCCC+6.02
KLF5MA0599.1chr6:43742693-43742703GCCCCGCCCC+6.02
MSCMA0665.1chr6:43744746-43744756AACAGCTGTT+6.02
MSCMA0665.1chr6:43744746-43744756AACAGCTGTT-6.02
MYF6MA0667.1chr6:43744746-43744756AACAGCTGTT+6.02
MYF6MA0667.1chr6:43744746-43744756AACAGCTGTT-6.02
SP3MA0746.2chr6:43742692-43742705CGCCCCGCCCCCC+6.11
ZNF263MA0528.1chr6:43742212-43742233TGGGGAGGAAGGGGAAGGGGC+6.48
ZNF263MA0528.1chr6:43743707-43743728GAGGGAGGAGTGAGGGGGAGG+6.86
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00396chr6:43736316-43745488Adipose_Nuclei
SE_01192chr6:43737139-43746428Adrenal_Gland
SE_23526chr6:43737293-43742678Colon_Crypt_1
SE_23526chr6:43742693-43743493Colon_Crypt_1
SE_23526chr6:43743674-43744675Colon_Crypt_1
SE_24121chr6:43742273-43743294Colon_Crypt_2
SE_24121chr6:43743834-43744202Colon_Crypt_2
SE_24895chr6:43737183-43743933Colon_Crypt_3
SE_24895chr6:43744129-43744674Colon_Crypt_3
SE_28417chr6:43733443-43743448Fetal_Intestine
SE_31486chr6:43733978-43746297Gastric
SE_40138chr6:43736992-43743467K562
SE_40138chr6:43744477-43745401K562
SE_40829chr6:43735857-43749621Left_Ventricle
SE_42766chr6:43736785-43746029Lung
SE_47663chr6:43741555-43743392Pancreas
SE_47663chr6:43743787-43744632Pancreas
SE_48225chr6:43736672-43749155Psoas_Muscle
SE_48830chr6:43735975-43746480Right_Atrium
SE_49610chr6:43742655-43743332Right_Ventricle
SE_51234chr6:43736064-43746936Skeletal_Muscle
SE_52912chr6:43736153-43744457Small_Intestine
SE_56485chr6:43735203-43744983u87
SE_56977chr6:43737921-43744654VACO_400
SE_60925chr6:43736759-43743185DHL6
SE_65246chr6:43735577-43753935Pancreatic_islets
SE_67504chr6:43735203-43744983u87
SE_69158chr6:43736725-43743662H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr64374273343743200
chr64374457543745076
Enhancer Sequence
ATCACGAAGG TGAGTCCCCC TGGCTGTTGG ATGGGGTTCC CTGTCCTCTC AGGGGATGGG 60
TGGATGGCCT AATTCCTTTT TCTTCAGAAC TGTGGGGAGG AAGGGGAAGG GGCACAGGAA 120
TATAAGGATC AAGAAAGAAA GAGCTGGGCA CCACGAGGTT CACCCTCAGT TTCGTGAGGA 180
CTCTCCGCTG TTCAGGTCTC TGCTAGAAGT AGGACTTGTT GCCTTTTTCT TCTGCTCTTT 240
CCAGTAAAAT TTTATTTGGA GAAGGAGTCG TGCGCACAGA GCAGGAAGAC AGTGTTCAGG 300
GATCCTAGGT GTTGGGGGAA GTGTCCCTTG TTTCCCCTAG CTCCCAGGGG AGAGTGGACA 360
TTTAGTGTCA TTTCCTATAT AGACATGTCC CATTTGTGGG AACTGTGACC CTTCCTGTGT 420
GAGCTGGAGG CACAGAGGGC TCAGCCTAAT GGGATCTCTC CTCCCTTCCC TGGTTTGCAT 480
TCCTTTGGGG GTGGAGAAAA CCCCATTTGA CTATGTTCGG GTGCTGTGAA CTTCCCTCCC 540
AGGCCAGCAG AGGGCTGGCT GTAGCTCCCA GGCGCCCCGC CCCCCTGCCC AACCCCGAGT 600
CCGCCTGCCT TTTGTTCCGT TGTGGTTTGG ATCCTCCCAT TTCTCTGGGG ACACCCTGGC 660
TCTCCCCACC ACTGACTGTG GCCTGTGCTC TCCACCTCTG GGGAGGGAAG GCCCTGGGGT 720
CTTCCTTCCC GCGAGTTTCC CTGACCTAAA TCTGGCGTGG CTGGGTAGTG GCCAGCAGTG 780
GTGATGCCCA GCCTGTTCTG CCTCCTCCTT CCCCACCCCA GGAGCCCTTT CCTTGGCCTA 840
GGACCTGGCT TCTCAGCCAC TGACCGGCCC CCTGCTTCCA GTGCGCCACT TACCCCTTCC 900
AGCTTCCCAG TGGTCTCTGG TCTGGGAGAG GCAGGACAAA GGTCTTTGTT TGCTGGAGAA 960
AAGGTTGTCT GCGATAAATA AGGAAAACCA CGAAAGCCTG GTTGTTGGAG TGTACGTGTG 1020
TGCTCCCCCA GGCAGTGGAG GCCAGCCCTC CTTGGAGGGG CGGCTGCCTG ATGAAGGATG 1080
CGGGTGAGGT TCCCCGCCTC CACCTCCCAT GGGACTTGGG GATTCATTCC AAGGGGAAGC 1140
TTTTTGGGGG AATTCCTACC CCAGGTCTTT TTACCCTCAG TTACCAACCC CTTGCCCAGG 1200
CCAGACCTTC CTGCTATCCC CTCCTGGGCC ACAAGCCTGG CCCTCCTCTG TCCCAATTGT 1260
GATGAAGGGG CAGTTCAAAA CTTCTTGATT AGTCATCTTC TCCCCTATCG ACTTGGCTTT 1320
AAAAAATGAC CTTTTCAGAC TTCTAGTCTC GTTCACTCTT TTTGATGATG CTTTGCCGTA 1380
ACCCTTCGTG GGTAGAGAAG GATTCTGTGC CCATTGGTGG TCTGGATAAA AGAAATAGAG 1440
ACCTCACAGG AAGCAGTGGA CTGGCCTGTT TCCCCACTGT TCTTTCTGTT TTCACACCTG 1500
TGGCCTTCTC CCCACCTTCT TCCCAATCAA CCTATTGTGT ACATAGCCCC CCTCATTGTC 1560
CTTTATTCTT CTGGAAAGCA GACCTTGGAG GGAGGAGTGA GGGGGAGGCT CAGCTGTGGT 1620
CTCTGGGGGG TGGGGGTTGG GAGCTGGGGT GGAAGTCCAC GAAGCATACA CTTAAGATGC 1680
TTTGGTGAAG TTCTAAACTT CATATTACCC AGGCTGAAAA AAGAGCACTT GTTCCTAGGG 1740
CTGGAAATGG AAGCCAAAAC ACCACCTTTT TCAGCCTGTT TCAGCATCTT TAGAGATCAG 1800
CCCAACCCAC TTACACAGTT GAGCAGAGTT GGAGGCCTAG AGAGGGGAGG GACTGGCCCA 1860
AGGTCATACC AACTCATGGC CAGAGCCTGG GCCTCCTCAC TGGCCAGGTG TTATTTCTTC 1920
CCTCTGGGTA GGGAACCTAT TTCAGGGACA GGATTGCTAT GTGGTAGTGG TGGTGGGGTG 1980
CGATAGGCGT GGCAGGCTGG GCCACAATTT GGAGTAGTCA TGCCAGAGTC CTGCATTTAT 2040
TTATTCTCAA GGGCCCCGCC TCTGTGGCCC AGAATTACCC CTTCATGCTC CAGTGCACCC 2100
CAGGCTTCGT GGCCAGCCTG GGAAACTGTC TCTACCCTGG TCTCCCTTCA GATCAGCTTC 2160
TAGAAATGTT TCGTGGCTAC AGTGGCAGCA CTGTTTTTTC CATGATGCAA GCAGTTTGCC 2220
CTCTTGGGCG GGGTTATCAG TGGCTGGCAG GGCTGGCACA GCGTGTCCGC CCACTGCCAC 2280
CTGTGGGTTC CAGGAGGGCC CAGCCCCTGT GCTGATGCCC ACCACCTTCT CAGCTCATGT 2340
CTGGGGAAGA GGACTGGCAG GGGGAAAGGT GCCTCCTCCT GAAAGGTGCC TCCTCTGTTT 2400
TTGCCTAATA TAGGCTTGGG AACACTTTGA TGTCAGCTAA TTCTGACTCC TTTACTTACT 2460
AGCTGTGCGG CCTTGGGGCA ACTTACTTAG CCTCTTTGAG CCTCCTGTTC CCCATCTGTA 2520
AAATGGAATC TCAATAGTGT CTAATAGTAC CATGTGGAGA AACTTGTGTG AAATGATAGC 2580
TGTGGACTAC TGTACACAGT ACTCAGGATG TAGTAAGTGC TCAATAAACA GCTGTTGGTA 2640
TGGTTGACGT TATGGTAGTG GTTGTGGGGA GGACGTAGGA AACTGGAGAC TAGCTTGGCA 2700
AAGCTGGCTC TTCCTCCTTT TAGGGAAAGC TTAGAGCATC CCCATGGGGT ATACCCATAC 2760
TCAGACTGTC CTCTGGCATC GAGGTTGGCC CAGGATTCAG TTCAGCTGTC ACAGTGAGGT 2820
GGCGGGATCA GATGTGGCAG GCCATGTCCC TTGGAACTTG AGTACATCGT GTGATCTCTG 2880
GAATGAAAAC AGGCCTTCAC CAGTGTTGAT GGTGGAAAGC TTAGGGAAGT GCTTCAAACA 2940
CAGTAGGAGG GACTTACGTT AGATTTTGGA AGGACTTGCC TGATTCGGAA GCTCCAAAGA 3000
GTGGCATTAC AGAGCTGGGT GGAGAGAGGG GCTAGCCATC TTTTGTGTCG CCCACCGGGC 3060
TCATGTGTCA TCGCCTCTCA 3080