EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS197-15618 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr4:6727550-6729440 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs73211754chr46729281hg19
TF binding sites/motifs
Number: 25             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr4:6728375-6728390TGACCTCCTGACCTC-7.19
RARAMA0729.1chr4:6728372-6728390TCTTGACCTCCTGACCTC-6.22
ZNF263MA0528.1chr4:6729346-6729367TCCTCCCCTTCCCCCTCCTCC-10.11
ZNF263MA0528.1chr4:6729358-6729379CCCTCCTCCTCCCCCTCCTTC-10.36
ZNF263MA0528.1chr4:6729349-6729370TCCCCTTCCCCCTCCTCCTCC-10.52
ZNF263MA0528.1chr4:6729406-6729427CTGTCCTCCTCCCCTTCCTTC-6.06
ZNF263MA0528.1chr4:6729410-6729431CCTCCTCCCCTTCCTTCCCCC-6.17
ZNF263MA0528.1chr4:6729372-6729393CTCCTTCTCCTCCCCTCCCCC-6.1
ZNF263MA0528.1chr4:6729384-6729405CCCTCCCCCTCCTCCCCCTCT-6.23
ZNF263MA0528.1chr4:6728662-6728683GGAGGAGGAGAGAAGGAAGAC+6.29
ZNF263MA0528.1chr4:6729331-6729352GTTCCCCCACTCCCCTCCTCC-6.2
ZNF263MA0528.1chr4:6729387-6729408TCCCCCTCCTCCCCCTCTCCT-6.47
ZNF263MA0528.1chr4:6729334-6729355CCCCCACTCCCCTCCTCCCCT-6.79
ZNF263MA0528.1chr4:6728659-6728680GGGGGAGGAGGAGAGAAGGAA+6.94
ZNF263MA0528.1chr4:6729343-6729364CCCTCCTCCCCTTCCCCCTCC-7.14
ZNF263MA0528.1chr4:6729355-6729376TCCCCCTCCTCCTCCCCCTCC-7.21
ZNF263MA0528.1chr4:6729397-6729418CCCCCTCTCCTGTCCTCCTCC-7.38
ZNF263MA0528.1chr4:6729340-6729361CTCCCCTCCTCCCCTTCCCCC-7.51
ZNF263MA0528.1chr4:6729367-6729388TCCCCCTCCTTCTCCTCCCCT-7.99
ZNF263MA0528.1chr4:6729409-6729430TCCTCCTCCCCTTCCTTCCCC-8.12
ZNF263MA0528.1chr4:6729378-6729399CTCCTCCCCTCCCCCTCCTCC-8.52
ZNF263MA0528.1chr4:6729381-6729402CTCCCCTCCCCCTCCTCCCCC-9.16
ZNF263MA0528.1chr4:6729352-6729373CCTTCCCCCTCCTCCTCCCCC-9.28
ZNF263MA0528.1chr4:6729364-6729385TCCTCCCCCTCCTTCTCCTCC-9.35
ZNF263MA0528.1chr4:6729361-6729382TCCTCCTCCCCCTCCTTCTCC-9.38
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr467287126729351
Number: 2             
IDChromosomeStartEnd
GH04I006727chr467289016729050
GH04I006728chr467290816729328
Enhancer Sequence
CATCACACAC AATCATACCA CACACGCATG CACACAACAC ACAATCATAC CACACACGCA 60
TGCACACACA TCACACACAA TCATACCACA CACACATGCA CACACATCAC ACACAATCAT 120
ACCACACACG CATGCACACA CATCACACAC AGTCATACCA CACACACATG CACACACATC 180
ACACACAGTC ATACCACACA CACATGCACA CACATCACAC ACAATCATAC TACACACACA 240
TGCACACACA TGCACACACA TCACACACAA TCATACCACA CACGCATGCA CACACATCAC 300
ACATAATCAT ACCACACACG CATGCACACA CATCACACAC AATCATACCA CACACGCATG 360
CAGACACAAC ACGTACACAT GCATGCATGC ATGTGTATCA CACACATTAC ACCACATATC 420
ACACATGCAC ACACAACACA CATCATGTAC ACACACGCCA CATACCACAC ACACAAACAT 480
TATGCACATA TGCATCCCAC ACATGCCTCA CACACACAAC GTACCACACA CACACACACA 540
CACACTGTGG TGATAAAATA CATGGGCATG GCATTCAGGC AGAGATTGGT TCCATCCCTG 600
TTCCATTTTT TTTTTTTTTT TCGGAGATGG AGTCTCGCAC TGTCACCCTG GCTGGAGTGC 660
AGTGGCGTGA TCTTGGCTCA CTGCAACCTC TGCCTCCCAG GTTCATGTAA TTCTCCTGCC 720
TCAGCCTCCC AAGTAGCTGG GATTACAGGT GCCCCCCACC ATGCCCAGCT AATTTTTTGT 780
ATTTGTAGTA GAGATGGGGT TTCACTATGT TGGCCAGGCT GGTCTTGACC TCCTGACCTC 840
GTGCCCACCT CAGCATCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCA CATCCAGCCT 900
CCTGTACCAT TATTTTACTA GCTGTGAATT TGGGCAAGTT ACTGGTGCTC TCTGACCCTC 960
AGTCTTTTTA TCTGCAGAAT GGGGTTACTC AAGGCACCTA CTTTCTGAAA TTGTTGGAGA 1020
GTCCTTGAGC TCAGGGGGCG AGGAGGACAG AGTTTTGTGA GGCACTATTC ACCTTTCAGT 1080
GGAAACATTT TTAATTTTGT TTCTGTCCTG GGGGAGGAGG AGAGAAGGAA GACTGGGGGT 1140
AAGTTCTCCC ACGTAAGACA GCTTCCTATG GACGATGAAT TTAGACTCGC CGCATCTGTG 1200
CATGCTCGTG TGGCCTCCCA GAGCCCGGGT GGCAGATGGG TGGCCTGGCG TGAGCATTCT 1260
TCGTTTCAGG CTGTGCCGGG CCTCCCCTTA ATAAAGACCT GTTTCTTCCC GGCTGCACTC 1320
TTGGCCCAGC CACCAAGGCT CAATGAGCTA TTCTGAGCTC CCGGCCTGCC CGCCGTGGAC 1380
ACACTCGGGC CTTCTGTTTG CCCACGGCCG CCCTGTGGGG CTTTCATAAA GCAGCCCTGT 1440
TCTCTCTCCC ACCGCGCAGC CGCCTGCTCC TTGGGGCCTT CTTAGGGAGG AGGCCGTGCC 1500
AGCCCGGGAG CCGGGGGCGT GGGGAGGCTG CGCTTTGCTG GCTTCCAGGA AGACGCACAC 1560
GCTGTGTGTG GCCAGAGACC GGGGCACCTC TTTGTTGGCG GCCCCATTGA CTTAGGGGCG 1620
ATTTGTTAGG GGTAAGACAC GTGTTCGGCG AGCAGGCTGC TGCTGCTCAC TCCCTTGAGA 1680
GAGGGCAGGC CTCCCTCTGG GATGCACGCT CACCAAGGCC ACAGGGTGCC GGGCCTTTGC 1740
ACGAGCTGTT CCTCTGATCT TCCTGGGGTG GCCTCCTCCT CGTTCCCCCA CTCCCCTCCT 1800
CCCCTTCCCC CTCCTCCTCC CCCTCCTTCT CCTCCCCTCC CCCTCCTCCC CCTCTCCTGT 1860
CCTCCTCCCC TTCCTTCCCC CACCCATCCT 1890