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

TagContent
EnhancerAtlas ID
HS176-20335 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr2:43395120-43396930 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr2:43396116-43396127CCACACCCTGC+6.62
RREB1MA0073.1chr2:43396606-43396626TGTCTGTGTGTGTGTTGTGG-6.01
RREB1MA0073.1chr2:43396608-43396628TCTGTGTGTGTGTTGTGGGG-6.54
ZNF263MA0528.1chr2:43396081-43396102TTTCCTTCCCTTTCTTCCTCT-6.18
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_03102chr2:43395315-43396058Bladder
SE_03102chr2:43396144-43397914Bladder
SE_09287chr2:43394591-43397814CD14
SE_10736chr2:43394904-43398818CD19_Primary
SE_11722chr2:43394406-43403989CD20
SE_11879chr2:43395778-43399784CD3
SE_13409chr2:43395012-43397907CD34_Primary_RO01536
SE_14384chr2:43395704-43399804CD4_Memory_Primary_7pool
SE_16655chr2:43396048-43398828CD4_Naive_Primary_8pool
SE_16950chr2:43396103-43398624CD4p_CD225int_CD127p_Tmem
SE_17323chr2:43394585-43404415CD4p_CD25-_CD45RAp_Naive
SE_17875chr2:43395625-43407220CD4p_CD25-_CD45ROp_Memory
SE_18565chr2:43394941-43399939CD4p_CD25-_Il17-_PMAstim_Th
SE_19552chr2:43395255-43399774CD4p_CD25-_Il17p_PMAstim_Th17
SE_20209chr2:43394960-43399771CD56
SE_20901chr2:43395401-43399064CD8_Memory_7pool
SE_22349chr2:43394743-43399769CD8_primiary
SE_23059chr2:43394803-43398677Colon_Crypt_1
SE_23724chr2:43394783-43398643Colon_Crypt_2
SE_24685chr2:43394825-43398672Colon_Crypt_3
SE_25333chr2:43394791-43398436DND41
SE_26374chr2:43395142-43397631Duodenum_Smooth_Muscle
SE_26557chr2:43394921-43398727Esophagus
SE_27617chr2:43394694-43399793Fetal_Intestine
SE_28536chr2:43394603-43399798Fetal_Intestine_Large
SE_30898chr2:43394882-43398155Fetal_Thymus
SE_31392chr2:43394985-43398655Gastric
SE_34919chr2:43394920-43397426HeLa
SE_38828chr2:43394545-43397667HUVEC
SE_40066chr2:43395750-43397271K562
SE_43203chr2:43394771-43398773Lung
SE_47826chr2:43395126-43397358Pancreas
SE_49954chr2:43396740-43397866RPMI-8402
SE_50052chr2:43394779-43398763Sigmoid_Colon
SE_52337chr2:43394808-43398777Small_Intestine
SE_53288chr2:43394791-43398735Spleen
SE_55101chr2:43394850-43397892Thymus
SE_56731chr2:43394807-43397647VACO_400
SE_58412chr2:43352450-43425007Ly1
SE_61450chr2:43354337-43468354Toledo
SE_62203chr2:43354169-43468733Tonsil
SE_65350chr2:43394818-43397799Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr24339649743396745
Number: 1             
IDChromosomeStartEnd
GH02I043167chr24339474143409195
Enhancer Sequence
CAGTTAGGTG ACCTGGGCAA TCCCCAGGCC TCTCTAAGCC TCAGTTTCCT GAGCTAGTGG 60
AAGCCCCTAG GTCACAGGGC TATTGTAGGG ATGGGTGTGC TCCTGAGGAA AACTAGCATG 120
AGCTTGGCAC CAGGCAGGTG AGGCCATGTG CTGCTCTCTG GGCCCCCAGC TTCTGTCCCC 180
CAGACCCTGG TGTCAGACAG GACCTGGTGA GAAATCCTTG CGGCCCTAGC CTGCCTAAGC 240
TGTGGAGGGG CTTGTCCAGG ACCTGCCAGG CAGAGGCTGC AGAAGGGTTC ACTTGGCCTT 300
TTCAGTCCCT CTCAGTCCCT TACTGTCTGC CTCTCAAGAA CATCCTGGCA CTTGCTGCTC 360
CACAGCCCTG CTGGGGTCCT GGGTGGGACT TTCTGGGGGC AGAGGAAGAA ATTCCAGGGC 420
CTGCCCTTGA CGAGCTCATA GTCTAACTGG GAAGAGAGTA GTGGCTCACT ATCCAGAAAA 480
CATGGAAAAG AGACTGTGGT TTGGAGAAAG CAGGAAGCGT TCAGAAGCGG GAGGCAGAAC 540
AGGGGAAGGC GCTGGAGCCT GAAGGATGGA GCGGACCAAG TGCAGAGGGG ATGGAGGGCA 600
CTGCAGGCAG GAGGCACAGC GAGAAGAATG GCCTGGAGGG TTGGATGGGG AACACGGGGT 660
CCTAGAGACG GAAGCAGGGT CCAGGCTGTG AGTGGTGGGG CCGCCTCAGC TGGGGAGTTA 720
TGGTAAGGAT AAACAGAAGG GCTCTGGGGC CGCCCAGAGT GCATACCCCC CAGGGTGCAG 780
ACGGGGGAAC AGCAATTGTC TCTGAGGGGG ATCCTCACCT CCCTATCTCA TCGGCCTAGG 840
AGACAGGACC TCACTTGACT GGCCCACAGC CAGGCCCTGG CTGTGTTGAC AAATGGGTCC 900
TTCCCCCTGG CCTGGTGAGC TGAGATGTGG CATTGTTAAG CTGCAAGTGA GTCACAGAAC 960
TTTTCCTTCC CTTTCTTCCT CTCTGCCCTG CTTGTCCCAC ACCCTGCTCA TTTTTTTTTT 1020
CTCTCTCTCT CTCTCTCTCT CACACACACA CACACACACA CACACTTGCC TTTCAGAACC 1080
TGTGAACTAT AAATAAGTGC TTTATCACCA TAAATGACTT GATCCAGGCT AGGGTCGTGA 1140
GGGGCTTGGC TCAGGTTCCT GGGCATGTGG ATACCTGCAG AGTGGGTTCC TGAGCACGTG 1200
AGGGCACAAG CGTGCAGTCT CGGACAAGGT GGAGTCTCAA TGTGTGAGCT TGCTGAGGCC 1260
AGGGCAGTGT CTGGGAAGGG AGTGGAGGCA TCTTTGTGTC TGTGGGGTTG TGGTGGGAGG 1320
GAGGTTTCGG GGGCTGTGAG GCGAGCACAG GCGTGTGTGC TGTCTATGCC CCCAAGGGGA 1380
CAGGGCGTGG GTGGAGAACG TATTTGTGCC CGAGGTGTGT CCGCAGGGAT ATCCGTGTGG 1440
TGAGTGTGGG AGGAGGGGCG CTGGGCATGG AGGAAGTGTT TCTGTCTGTC TGTGTGTGTG 1500
TTGTGGGGGT GGCGGGGATT GGCGGGGGTG GGTTGTGCCT GGCCAGCCAA CCTTTACATC 1560
TGGTTCTGCA GGATGTGAAA AGGTTTGTGA CTGAGGCCAG TGGCACACCC TCCAGTCGGA 1620
TCAGAGGGTT GGAGATAAAC CCAAGTGAGC AAGCATTGGT GGCTGTGGCC GTGTGGTGTC 1680
CCATTCCTGG GGGGCTCCAG GAGATAGGGA AGCTCATCTG ACTTCCTGAG GGCCTGGCAG 1740
CCCCTCCTGC CCTCCTCAAG GTGGTCCATC TGCCACGCCA AGCCCAGCCA GAGAGAAGGG 1800
GCACCCGGAG 1810