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

TagContent
EnhancerAtlas ID
HS194-02955 
Organism
Homo sapiens 
Tissue/cell
Urothelial_cell 
Coordinate
chr2:43395390-43396830 
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_12501chr2:43396298-43396478CD34_adult
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_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
CAGAGGCTGC AGAAGGGTTC ACTTGGCCTT TTCAGTCCCT CTCAGTCCCT TACTGTCTGC 60
CTCTCAAGAA CATCCTGGCA CTTGCTGCTC CACAGCCCTG CTGGGGTCCT GGGTGGGACT 120
TTCTGGGGGC AGAGGAAGAA ATTCCAGGGC CTGCCCTTGA CGAGCTCATA GTCTAACTGG 180
GAAGAGAGTA GTGGCTCACT ATCCAGAAAA CATGGAAAAG AGACTGTGGT TTGGAGAAAG 240
CAGGAAGCGT TCAGAAGCGG GAGGCAGAAC AGGGGAAGGC GCTGGAGCCT GAAGGATGGA 300
GCGGACCAAG TGCAGAGGGG ATGGAGGGCA CTGCAGGCAG GAGGCACAGC GAGAAGAATG 360
GCCTGGAGGG TTGGATGGGG AACACGGGGT CCTAGAGACG GAAGCAGGGT CCAGGCTGTG 420
AGTGGTGGGG CCGCCTCAGC TGGGGAGTTA TGGTAAGGAT AAACAGAAGG GCTCTGGGGC 480
CGCCCAGAGT GCATACCCCC CAGGGTGCAG ACGGGGGAAC AGCAATTGTC TCTGAGGGGG 540
ATCCTCACCT CCCTATCTCA TCGGCCTAGG AGACAGGACC TCACTTGACT GGCCCACAGC 600
CAGGCCCTGG CTGTGTTGAC AAATGGGTCC TTCCCCCTGG CCTGGTGAGC TGAGATGTGG 660
CATTGTTAAG CTGCAAGTGA GTCACAGAAC TTTTCCTTCC CTTTCTTCCT CTCTGCCCTG 720
CTTGTCCCAC ACCCTGCTCA TTTTTTTTTT CTCTCTCTCT CTCTCTCTCT CACACACACA 780
CACACACACA CACACTTGCC TTTCAGAACC TGTGAACTAT AAATAAGTGC TTTATCACCA 840
TAAATGACTT GATCCAGGCT AGGGTCGTGA GGGGCTTGGC TCAGGTTCCT GGGCATGTGG 900
ATACCTGCAG AGTGGGTTCC TGAGCACGTG AGGGCACAAG CGTGCAGTCT CGGACAAGGT 960
GGAGTCTCAA TGTGTGAGCT TGCTGAGGCC AGGGCAGTGT CTGGGAAGGG AGTGGAGGCA 1020
TCTTTGTGTC TGTGGGGTTG TGGTGGGAGG GAGGTTTCGG GGGCTGTGAG GCGAGCACAG 1080
GCGTGTGTGC TGTCTATGCC CCCAAGGGGA CAGGGCGTGG GTGGAGAACG TATTTGTGCC 1140
CGAGGTGTGT CCGCAGGGAT ATCCGTGTGG TGAGTGTGGG AGGAGGGGCG CTGGGCATGG 1200
AGGAAGTGTT TCTGTCTGTC TGTGTGTGTG TTGTGGGGGT GGCGGGGATT GGCGGGGGTG 1260
GGTTGTGCCT GGCCAGCCAA CCTTTACATC TGGTTCTGCA GGATGTGAAA AGGTTTGTGA 1320
CTGAGGCCAG TGGCACACCC TCCAGTCGGA TCAGAGGGTT GGAGATAAAC CCAAGTGAGC 1380
AAGCATTGGT GGCTGTGGCC GTGTGGTGTC CCATTCCTGG GGGGCTCCAG GAGATAGGGA 1440