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

TagContent
EnhancerAtlas ID
HS155-11437 
Organism
Homo sapiens 
Tissue/cell
Ovary 
Coordinate
chr5:131832560-131834040 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs736801chr5131833599hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF8MA0652.1chr5:131832714-131832728GGTTTCGGTTTCTT-6.09
IRF9MA0653.1chr5:131832714-131832729GGTTTCGGTTTCTTG-6.07
KLF5MA0599.1chr5:131832607-131832617GGGGCGGGGC-6.02
Number of super-enhancer constituents: 46             
IDCoordinateTissue/cell
SE_00037chr5:131820679-131837440Adipose_Nuclei
SE_04124chr5:131829583-131834782Brain_Anterior_Caudate
SE_06435chr5:131828999-131837748Brain_Hippocampus_Middle
SE_09163chr5:131829465-131834473CD14
SE_10340chr5:131828916-131834254CD19_Primary
SE_10915chr5:131818633-131838738CD20
SE_11856chr5:131829481-131834757CD3
SE_13479chr5:131829083-131833511CD34_Primary_RO01536
SE_14495chr5:131829023-131834270CD4_Memory_Primary_7pool
SE_15423chr5:131830722-131833719CD4_Memory_Primary_8pool
SE_16304chr5:131830422-131833644CD4_Naive_Primary_8pool
SE_16894chr5:131829085-131834220CD4p_CD225int_CD127p_Tmem
SE_17370chr5:131818848-131837330CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131818558-131837415CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131818792-131837424CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131828766-131834527CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131828783-131837777CD56
SE_20775chr5:131829020-131834036CD8_Memory_7pool
SE_21523chr5:131829420-131833537CD8_Naive_7pool
SE_21960chr5:131829489-131833482CD8_Naive_8pool
SE_22284chr5:131818534-131837164CD8_primiary
SE_23079chr5:131830842-131839811Colon_Crypt_1
SE_23750chr5:131830830-131834331Colon_Crypt_2
SE_25340chr5:131829511-131832754DND41
SE_25784chr5:131828604-131839493Duodenum_Smooth_Muscle
SE_26597chr5:131829568-131834655Esophagus
SE_27629chr5:131830752-131839506Fetal_Intestine
SE_28559chr5:131830527-131839276Fetal_Intestine_Large
SE_30917chr5:131829648-131834047Fetal_Thymus
SE_31393chr5:131829777-131839489Gastric
SE_39368chr5:131832650-131834315Jurkat
SE_40726chr5:131829734-131835879Left_Ventricle
SE_42103chr5:131829574-131839460Lung
SE_44054chr5:131830691-131837759MM1S
SE_47919chr5:131830793-131834371Pancreas
SE_48659chr5:131829847-131835640Right_Atrium
SE_50051chr5:131828811-131839642Sigmoid_Colon
SE_52336chr5:131828839-131839793Small_Intestine
SE_53285chr5:131829513-131839339Spleen
SE_54554chr5:131829395-131838583Stomach_Smooth_Muscle
SE_57943chr5:131830882-131833250VACO_9m
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131830099-131835199Pancreatic_islets
SE_66244chr5:131832650-131834315Jurkat
SE_67186chr5:131830691-131837759MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr5131832561131832909
chr5131833441131833717
chr5131833002131833333
Number: 1             
IDChromosomeStartEnd
GH05I132493chr5131828971131839447
Enhancer Sequence
GGCACTCAGA TGGCTCCCAC CTCCGCCTGG GCCTTGCAGC TGGCGGTGGG GCGGGGCGCA 60
GGGGCCGGGT AGGGGAGGGC TTGGGTCCGG CCATCCAGTG GGGGTCAGCC CCATCGCCGG 120
GTTCCGCGGG GCCGCGCCGA AGGGGCGGAG CCTGGGTTTC GGTTTCTTGC AAACGCGGCG 180
GCAACAGGGA AATCGAGGAG TTTCCGGGAA CCGAACCACG CTGGGAGCGC TGAGGTCTGC 240
GCAGCGGCGG GGGCCGGGGG ACGGGCGGGC GTCCAGTGTT ACCGGCCAGT GGCCAGCTGG 300
AAGTTCCAGC GGGAGCCGGG GAAAACCGGC CCCGGAAAAG CCCCACCTGA ATGCACCTGC 360
CCAGGCCTCT CCGGATGGTG TTCATGCTGA GGGTGGGGGT GTGAAGGATG GACCTGCCTG 420
CAGGGTGGCC TTTAGGGAAT GAGGGAGGAG TTCTACAAGC TAAGGGGTTT GAGGGTGTGC 480
ACGCGGGGAA AGAGGGGACT GTGCGCAGGC AGGTGGGATC TGAGGAATTG GGATATCCCC 540
TCAAATGACT GAGGTCCCCA GCTGTCCCCT CACTGTCACA TCCCATCTTA TTGTCCTTAT 600
ACGATGAGGT CTCCTTACTG AGATCATATC CGTAGTGTCC TCTTTTGCTT ATTTGTTGGA 660
GGATTTCCCC GAACATGACT TGGAGCCCTT GAGAGTGAGC CCTGACTGTC TGGTCTAGTC 720
TCCTGGATCT AGAACCCACC AACCTCCACG GGGGGCTTGT GACTGTTTAC TAAGTGAGAA 780
AAGGAGTAGG GTGAGTTCGA GGCATCTGTG AGGTCCATAT GCCTTCTGAC CTGCTCCCCC 840
ACAGGACCCC TAGCCCACTC AGGTCCTGCC ATGTCCCCAG TTGAAGGAAG CCCCACTCTG 900
CAGAAGATGC CTTGGCTTTT GTGGGAGGGG CTTCCCTTGT AGTTCCCTGA GAACTGCCTT 960
CCAGCTGGGA TGGCTGGGCA GAAGGCGGAC TGTAGTCATC ACAGAGGAAT GCTGGCCGTG 1020
GGGTCAGCCA CTTCCTTCCC TCCCCAGGGC TTGGAGCTCA GGCCAGGGAT TATGGTGGGT 1080
TGGCCCTGGA TCTGAGACAA GAAGGCTGGG AGTTTGGGTG GCAGAGGGAG AGTCCAGTAC 1140
CCTCCCTGAT CTCTGCAGCC CACAGCAGTA CCTGGGGTCA AGGTGGACAG TGTCACTGGC 1200
AAGCCCATGT TTCCTAAATG CATGCCTTTG AGACCACAAG TCTATGGTAA GGATCTCTTT 1260
CCTTATGGCC CTGAGACCAT GGCTCTTGGA AAGACATAAA TCAGACTAAA TGGAGCTCCC 1320
TCAGCCCAGA AGAGCTGGGG CTGGGGCAGG TATCAGTGGT GGCTATTCTG GAAGCAGCCA 1380
GCTAGCCAGT GGAAGGAGAG GCAGCAAGAC CTCCCTAGCA TCCCTGTATG GGCCAACACT 1440
GACTTTCACC AGCCCAGGCT TAGGATCAGG GTGGCTGGCC 1480