EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS151-08103 
Organism
Homo sapiens 
Tissue/cell
OCI-LY1 
Coordinate
chr3:13050700-13052130 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ELK1MA0028.2chr3:13051753-13051763CACTTCCGGT-6.02
ERGMA0474.2chr3:13051753-13051763CACTTCCGGT-6.02
ETS1MA0098.3chr3:13051753-13051763CACTTCCGGT-6.02
FEVMA0156.2chr3:13051753-13051763CACTTCCGGT-6.02
FLI1MA0475.2chr3:13051753-13051763CACTTCCGGT-6.02
ZNF263MA0528.1chr3:13051084-13051105CCCTCATCCCTCACCTCCTCC-7.31
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_04670chr3:13051925-13052877Brain_Anterior_Caudate
SE_08605chr3:13050920-13052130Brain_Inferior_Temporal_Lobe
SE_09375chr3:13049364-13059639CD14
SE_10176chr3:13046655-13065411CD19_Primary
SE_10911chr3:13035699-13066171CD20
SE_11922chr3:13049781-13059045CD3
SE_14626chr3:13048295-13060160CD4_Memory_Primary_7pool
SE_15585chr3:13050195-13051944CD4_Memory_Primary_8pool
SE_16175chr3:13051230-13052024CD4_Naive_Primary_7pool
SE_16432chr3:13050005-13054882CD4_Naive_Primary_8pool
SE_17019chr3:13050223-13054537CD4p_CD225int_CD127p_Tmem
SE_17506chr3:13048647-13059751CD4p_CD25-_CD45RAp_Naive
SE_17882chr3:13048254-13059646CD4p_CD25-_CD45ROp_Memory
SE_18733chr3:13049856-13059008CD4p_CD25-_Il17-_PMAstim_Th
SE_19289chr3:13049944-13058908CD4p_CD25-_Il17p_PMAstim_Th17
SE_19986chr3:13042696-13060659CD56
SE_20899chr3:13048928-13059283CD8_Memory_7pool
SE_21767chr3:13050064-13059216CD8_Naive_7pool
SE_22232chr3:13049924-13059169CD8_Naive_8pool
SE_22360chr3:13049286-13059937CD8_primiary
SE_24441chr3:13050345-13050945Colon_Crypt_2
SE_24441chr3:13051234-13051574Colon_Crypt_2
SE_32449chr3:13050449-13051096Gastric
SE_32449chr3:13051127-13051622Gastric
SE_32598chr3:13049773-13064792GM12878
SE_43204chr3:13050220-13052698Lung
SE_43685chr3:13049159-13061365MM1S
SE_50528chr3:13049434-13060971Sigmoid_Colon
SE_53233chr3:13049849-13059374Small_Intestine
SE_53444chr3:13049476-13061207Spleen
SE_58860chr3:13034529-13067396Ly3
SE_61934chr3:13035948-13071595Toledo
SE_62359chr3:13034207-13065666Tonsil
SE_67345chr3:13049159-13061365MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr31305088513051150
chr31305126113051495
Number: 1             
IDChromosomeStartEnd
GH03I013001chr31304333013065896
Enhancer Sequence
CCAGAGAGGC CTGGTGACTC GCCCTAGGTC ACACAGTGCG GTGACAGCCA ATCCAGGACC 60
GGTGCCCGGA CTGCCACACC TCTCCATGTG GTGGCGGTGA AGCTAAATGG CCTGCTGCCT 120
TGATTTCCCC TTTGTGCCAT GAGGGTGTGG GCAGGCTGAT TTCTGACATG GTGTAATGTC 180
ATCAGGGAGG CGGGACCTTG CCTGAGAAGC CTTAGGGCTG AAAAGGGAAG CGCAGAGTGG 240
CTGTTTCCCC ATCCTGCCCG CTCTCCGCCC TGGCCCTGAG CCAGGTGGGC GGCCAACTCC 300
CTTTGACCAC TTCCTGGGGT AACTCCCCCG GAAATGCCCC AGATGCCCGC AGCCCAAGTA 360
TAACTCCAAC TTCCAGGCTC AGGACCCTCA TCCCTCACCT CCTCCTGCCA AGATCACCCC 420
AAGCAGAAAC CAGTAGGCAT AATAATTAGT ATGTTTGTAT ATATATATGT GTGTGTGTGT 480
GTGTGTGTAT GTACTTTGCT GATTAGATAT TTTATCAGAT ATCTTATCTA TATAAGGAAA 540
CAACAACAAA AGTGAAGCTG ACAGTGCGTT GAGAGCCGGG CTTTAGCACA CCACAGCTCT 600
ATGTCTTAGG ATCCCTCCTC TCTGCCAGTG TGGCGCCCGC CTCCTACTCC CATCCTCTGC 660
CTCCAGTCTC CTCTGCCAGC CTGTCCTCCA TCCAAGCTCC CTAGGCATCC TCTTCAAACT 720
CTTTGCTGAT TGCTGTAAGG CAGTGGAGCA TGTGGTTAAG ATTCTGGGCT TCAGGTCAAG 780
CTGATTTGGG ATTTGAGGAC ATTTGCTAAC AGTGTGACCT TCGGCAAGTG ACTGTGTCTC 840
CCTAAGCCTC AGTTTTCTCA TCTGCAAAAT AGGGATCATA ACAAACTCTA CCTCACGGGG 900
CTGACCCGAA GGGATGATGC ATAGCAGAAC ACATGGCTCA GCTGGCCAGC CGGCAGGTCT 960
TAGCAGGTCA TAGTGGCGGA ATGACCAGCC CACAAGTCTT AGCAGGTCGC AATGGTGGAT 1020
GCAGGATGTT TCTGCCTGAC CAGCCTCCAT TCTCACTTCC GGTAAGACAC CCCAATTTTC 1080
TTTGGGGAAT CCAATCCTCC ATTCTCAGTC CATCTAATTT GGGTCAGCTA CCTCCAGGGG 1140
TGAATGCAGT ACCGAGCTTG GTCTATCAGA GAGAGTAGTT CATCCCCCCT GCTCAAGTGA 1200
CTGGTCCAGG GATGGGTATG TGGTCTAAGC TAACCATGGA GAGTCGATTC TGTCAGAACA 1260
GTTTCTGCCT GGATATGACA AATGTCGACC TGGAGCTGTT GGGGCCATCT GGGCAGAAAG 1320
GCTGTCCGGG AATGAAGTCA AAGAGATGGA AAAAGAGAAA AAGAGGCCGG CGTCTGGGGT 1380
CATGGTTTGA GCCCCCGAAT CCAACTGTAC CTGAAGCCCT GTCTGTTTCA 1430