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

TagContent
EnhancerAtlas ID
HS044-13242 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr9:33160540-33161950 
Number of super-enhancer constituents: 51             
IDCoordinateTissue/cell
SE_00330chr9:33154468-33169472Adipose_Nuclei
SE_00992chr9:33160418-33162204Adrenal_Gland
SE_03080chr9:33160872-33162102Bladder
SE_09459chr9:33152609-33169475CD14
SE_10229chr9:33152539-33167365CD19_Primary
SE_10912chr9:33119344-33169982CD20
SE_12090chr9:33157738-33162237CD3
SE_14891chr9:33157888-33169405CD4_Memory_Primary_7pool
SE_16667chr9:33158291-33160788CD4_Naive_Primary_8pool
SE_17238chr9:33158125-33162210CD4p_CD225int_CD127p_Tmem
SE_18081chr9:33156865-33169734CD4p_CD25-_CD45ROp_Memory
SE_18665chr9:33152608-33169527CD4p_CD25-_Il17-_PMAstim_Th
SE_19329chr9:33157783-33168754CD4p_CD25-_Il17p_PMAstim_Th17
SE_20045chr9:33157602-33169486CD56
SE_21266chr9:33157965-33160951CD8_Memory_7pool
SE_21892chr9:33157533-33160719CD8_Naive_7pool
SE_22416chr9:33156349-33169559CD8_primiary
SE_23687chr9:33160317-33164381Colon_Crypt_1
SE_26031chr9:33156101-33167436Duodenum_Smooth_Muscle
SE_26859chr9:33157850-33169485Esophagus
SE_27770chr9:33157683-33167402Fetal_Intestine
SE_28724chr9:33157899-33168754Fetal_Intestine_Large
SE_29800chr9:33156282-33168738Fetal_Muscle
SE_31534chr9:33160292-33169401Gastric
SE_32659chr9:33157722-33167394GM12878
SE_34775chr9:33156270-33169231HeLa
SE_36192chr9:33157786-33167403HMEC
SE_40894chr9:33157797-33168888Left_Ventricle
SE_41831chr9:33160938-33164553LNCaP
SE_42236chr9:33157802-33169593Lung
SE_44340chr9:33158046-33163936NHDF-Ad
SE_45447chr9:33158228-33162713NHLF
SE_45731chr9:33156466-33167394Osteoblasts
SE_46917chr9:33160893-33162119Ovary
SE_47814chr9:33160981-33161787Pancreas
SE_48426chr9:33160333-33168885Psoas_Muscle
SE_48738chr9:33160772-33168636Right_Atrium
SE_50176chr9:33157791-33169402Sigmoid_Colon
SE_51651chr9:33154916-33168964Skeletal_Muscle
SE_52621chr9:33157845-33169145Small_Intestine
SE_53402chr9:33157750-33169185Spleen
SE_55540chr9:33160440-33160822Thymus
SE_55540chr9:33160833-33162885Thymus
SE_56627chr9:33157705-33163591u87
SE_57910chr9:33160466-33161121VACO_503
SE_57910chr9:33161174-33161748VACO_503
SE_57910chr9:33161805-33162823VACO_503
SE_58985chr9:33124740-33168862Ly3
SE_62118chr9:33106994-33169093Toledo
SE_62346chr9:33106942-33169226Tonsil
SE_64585chr9:33157718-33167337NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr93316094433161390
Enhancer Sequence
AATCACTTGA GCTCTGGAGT TCGAGACCAG CCTAGGCAAC ATGGCAAAAC CCCATCTCTA 60
CAAAAAATAC AAAAATTAGT CAGGCATGGC GGTGTGCACC TGTGGTCCCA GCAACTCGGG 120
AGACTGAAGT GGGAGAATCG CTTAGCCCGA GAGGTCGAGG CTGCAGTGAG CCGTGATCAC 180
TGCACTCCAG CCTGGGTGAC AGAGCAAAAA CCCTGTCTCA AAAAGAAAAA GAAAAAAAAA 240
TATATCAGCT ATATTCTTAA ACATGAAAAA GACTAGTAGG AAATATGCCG GTATGTTTCT 300
TTTGGGTGAT AGGAATTTGG GTGTGCTTTT ATATCTCTTT CAACTTTTCA AATTATTTTC 360
AATGAGCCTG CATTACTTTT TACTTTTAAA ATGAAGGAAG AGATTATCCC CCCTCAAAAG 420
GCAAAAGCAA AGACCCATAC CCCTATCCCT ATCCCCAACA TCTCTGTGAG GCAAGTCATT 480
CTCTCTCTCT CTCTCTCTCT CTCTGCCTGG GCTTTGTGAG GGGCTCTGGA GAAGCAGCGG 540
GTGTGGGGAG TGGATAGAGA AGCAGCTACA TAACACACCC AGACCAGACT TTAAAATCAC 600
TGCCAAAGAA TTCAGCAACA GCCAATTATA TAGCCCCTGG CCTTCATTTG TGCAGGGAAG 660
GGGCGGGCTG AGGCCAAGCC GCAAAGTGGA ACCTGAAGCA CTGAGTGTGT GACTCACCCC 720
TCTGTCTTCT AAGGACAAAT CCCTTTAGGC CACATTCACC CAGAACCAGC TCCCCACTAA 780
ACCCTGTCCC CCACCCCCAA GCCCCACTCT CCAACCTGGA GGTCTCTGAC TTACAGAACA 840
ATATCCTGAG ATCACTCCTT GAGCTAGTGA CCGCCTCAGC TCACCCGGCA ATGGCCCAGA 900
TCAACACAGA GGCCCCTACA ACTCAGGTCT CAGGTCTCTA CAATCTTAAT CGCAGTCTGG 960
CTCCCAGGAA CCCCTACCAA GTTTAGGGAC AGGAGGGACC CTGTGAGTCT AATCCCATGC 1020
CTTGTTAATT CCCCTAGGAG CCAGGGTCTG GCTGGCTGGC CTTACAGTGA CCTCACTGCC 1080
CAGGGACCAC ACCAGTCTAT ACCAAAGCCA AATGTAAAAC TGTCACCATG CCAGGCCCTC 1140
AAAGGATTTA AGCTTCAAGG GCAGACCATT TGTCCTAAAA CAACTGGATT GCTGCTCCAC 1200
TGGACAAGAA AAACTGGAAT TTCCAGGTAG ATGTGGGTTC AAGCAGAATT CCAGTCTCTG 1260
CTTCTTCATA GTAAGAGCAG AGAACAAAGA GTAAGAAACA AGGTACAGGA GGCACTGGGT 1320
AAACAGATAG CAGGGAAATC AGCAGGTATG ACTACTGAAT AAACCTCTTT CACAAACACA 1380
CACCCATAGC CCAGCTGAGT GCAAAGGGGA 1410