EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS151-00173 
Organism
Homo sapiens 
Tissue/cell
OCI-LY1 
Coordinate
chr1:23894190-23895240 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NHLH1MA0048.2chr1:23894671-23894681CGCAGCTGCG+6.02
NHLH1MA0048.2chr1:23894671-23894681CGCAGCTGCG-6.02
ZNF263MA0528.1chr1:23895155-23895176CCCCTATTCTCGTCCTCCACC-6.03
ZNF263MA0528.1chr1:23894480-23894501TTTTCCTCCACTCCCTCACCC-6.11
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_01721chr1:23894114-23896139Aorta
SE_02313chr1:23894629-23895597Astrocytes
SE_02990chr1:23894236-23895942Bladder
SE_03649chr1:23894865-23896346Brain_Angular_Gyrus
SE_04396chr1:23893786-23894682Brain_Anterior_Caudate
SE_04396chr1:23894689-23896647Brain_Anterior_Caudate
SE_05716chr1:23894706-23896744Brain_Cingulate_Gyrus
SE_06239chr1:23879137-23896940Brain_Hippocampus_Middle
SE_07293chr1:23893676-23896957Brain_Hippocampus_Middle_150
SE_08579chr1:23894669-23896816Brain_Inferior_Temporal_Lobe
SE_09076chr1:23895058-23895569Brain_Mid_Frontal_Lobe
SE_10300chr1:23893905-23894618CD19_Primary
SE_10300chr1:23894638-23895218CD19_Primary
SE_11050chr1:23891759-23895821CD20
SE_15327chr1:23894282-23896070CD4_Memory_Primary_7pool
SE_23281chr1:23894157-23895276Colon_Crypt_1
SE_23782chr1:23894110-23895236Colon_Crypt_2
SE_24936chr1:23894139-23895632Colon_Crypt_3
SE_26335chr1:23894950-23895988Duodenum_Smooth_Muscle
SE_27258chr1:23894169-23895985Esophagus
SE_27884chr1:23894178-23896122Fetal_Intestine
SE_28880chr1:23894076-23896000Fetal_Intestine_Large
SE_29676chr1:23894052-23896300Fetal_Muscle
SE_31953chr1:23894148-23896022Gastric
SE_33209chr1:23894237-23895252H1
SE_37153chr1:23894617-23895647HSMMtube
SE_38016chr1:23894037-23895844HUVEC
SE_41075chr1:23894073-23896242Left_Ventricle
SE_42328chr1:23893887-23896240Lung
SE_45797chr1:23894474-23895828Osteoblasts
SE_48755chr1:23893984-23896237Right_Atrium
SE_50077chr1:23893624-23896094Sigmoid_Colon
SE_52549chr1:23894058-23895971Small_Intestine
SE_53706chr1:23893935-23895950Spleen
SE_54840chr1:23894330-23896020Stomach_Smooth_Muscle
SE_55341chr1:23894275-23895143Thymus
SE_56054chr1:23894210-23895677u87
SE_58372chr1:23873313-23964782Ly1
SE_68324chr1:23879596-23905390TC32
SE_68325chr1:23879596-23905390TC32
SE_68477chr1:23874949-23904689TC71
SE_68478chr1:23874949-23904689TC71
SE_69046chr1:23893964-23895982H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12389453223894693
Number: 1             
IDChromosomeStartEnd
GH01I023567chr12389349223896026
Enhancer Sequence
ACCGCGCCCG ACCTCAGTTT CTGAGTGTAT TCCTACCTGA GAATATGCTG TCCACCCTTG 60
TCTGAGTGTG GGGCTGTCCT TGGGGGCTGT GCGCGGGGTG CGCCTATGTG TCTTCCTCCC 120
TGGGTGTTTC AGCCTGCTGT GTGTGATGTG TCCCCGGGTC TAGTATAGGA TCTTCCCTGG 180
GTGTGCGGCT TTCTATGTGC GTGCTTCAGT GTATGTCCAT CTTCCCCCAA TCTCCTAGCC 240
AGGTGCGGAA CAGGGCCAAG AGGACAATAG GCTCGAGCGC CCAGGTGGCC TTTTCCTCCA 300
CTCCCTCACC CACCGCGACC CTCCCCTCCT GCACCCCGCG CCCTGACTGC CCCCTCTCTG 360
GCCCTGCCCG ACCTTCCGCG GCCCTCCCTG CCCGCGCCCC GGCGGCCCCA CCCTGGCCCT 420
ACCCGGCCCT CCCCGCCCGC GCCCCGCGCC CGGCGGCCCC AACCCCCGGC GGTCCCGGAC 480
GCGCAGCTGC GGGACACACA ATCGCCGGCG CCCCCTCTCC GCCCCCCGCG CAGCCCCTCG 540
TCCAACAAAA GCCGCTTTCT TTCCCCACAA CAGATTAAAG ACCAGGAGGG GGTGAAAAAT 600
AGCTTCTCCG GCCACTGGCG GGGGAGGGGC GCGGGAAAAG CTGGGACTTT GGGGACTCTT 660
TGATAGCGAG TGTGTGGGAA ACCCGAAGGA ATGTGGCTGT TCGGACCGCC GCGGCGGGGC 720
CAGGCGCCGG GAGGAGGGTC CGCACCTCCC CCGCTGGGAC TCCCGGGACC TCCCGGACCC 780
CCGCGGCCCC AGCGTCCCTG CGGCCCCGGC GTCCCCACGC CCCACGCCGC CAGCGCCCTG 840
CACGCCGCCT CCCGCCAGCT GAGCGTCTCC CGCGCCCCCT GCTTTTCCTC CCCTAGTCAA 900
TTTCCTCACA TTCTAATTTC CTTACTTTCT TCTCACTTTC CCTTCCAATT CTCCTTTTCG 960
CGAGTCCCCT ATTCTCGTCC TCCACCTCTT TCTCTATGTC TTTTGCTCAA GTCTGTTCCC 1020
CTCGTCTCCC TCCCCGGGTC TTTATCTTGA 1050