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

TagContent
EnhancerAtlas ID
HS176-00384 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr1:23902880-23904600 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata1MA0035.3chr1:23902982-23902993ACAGATAAGGA-6.14
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_01721chr1:23900657-23905229Aorta
SE_02313chr1:23901876-23905526Astrocytes
SE_02990chr1:23903287-23903795Bladder
SE_03649chr1:23903331-23903843Brain_Angular_Gyrus
SE_03649chr1:23903960-23904459Brain_Angular_Gyrus
SE_04396chr1:23902891-23904726Brain_Anterior_Caudate
SE_05716chr1:23903816-23905335Brain_Cingulate_Gyrus
SE_06239chr1:23900696-23905116Brain_Hippocampus_Middle
SE_07293chr1:23902637-23904795Brain_Hippocampus_Middle_150
SE_08579chr1:23902794-23905344Brain_Inferior_Temporal_Lobe
SE_10300chr1:23899372-23906111CD19_Primary
SE_11050chr1:23898822-23908436CD20
SE_18996chr1:23902922-23905455CD4p_CD25-_Il17-_PMAstim_Th
SE_26335chr1:23902515-23905797Duodenum_Smooth_Muscle
SE_27258chr1:23902880-23904675Esophagus
SE_27884chr1:23903017-23904621Fetal_Intestine
SE_28880chr1:23903194-23904813Fetal_Intestine_Large
SE_29676chr1:23901788-23905238Fetal_Muscle
SE_31953chr1:23902935-23903813Gastric
SE_31953chr1:23903835-23904596Gastric
SE_34689chr1:23902272-23905407HeLa
SE_37153chr1:23901250-23906299HSMMtube
SE_38016chr1:23903113-23904896HUVEC
SE_38999chr1:23901867-23905446IMR90
SE_41075chr1:23901556-23905295Left_Ventricle
SE_42328chr1:23901634-23904721Lung
SE_44435chr1:23902863-23905477NHDF-Ad
SE_45797chr1:23901058-23906146Osteoblasts
SE_48755chr1:23902917-23904674Right_Atrium
SE_50077chr1:23902728-23906171Sigmoid_Colon
SE_51741chr1:23901781-23905632Skeletal_Muscle_Myoblast
SE_52549chr1:23902842-23905170Small_Intestine
SE_53706chr1:23902697-23905306Spleen
SE_54840chr1:23900793-23905744Stomach_Smooth_Muscle
SE_55341chr1:23903385-23903804Thymus
SE_55341chr1:23903829-23904379Thymus
SE_56054chr1:23901526-23905401u87
SE_58372chr1:23873313-23964782Ly1
SE_63528chr1:23901642-23905713HSMM
SE_68324chr1:23879596-23905390TC32
SE_68325chr1:23879596-23905390TC32
SE_68477chr1:23874949-23904689TC71
SE_68478chr1:23874949-23904689TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12390371423904323
Number: 1             
IDChromosomeStartEnd
GH01I023572chr12389942723906089
Enhancer Sequence
TATATTTTTA GCAAACATTC ATGTAACACT ATGTGCCAGG CACCATTCTA AGTGCTTTAC 60
AAATGTTTAT TTAGGTAACA GAGGTACTGT TGCCTCCATT TTACAGATAA GGAAACTGAG 120
ACACAGAGAG GCTAATTTGC CCAAGACCAC GTGGCTAGCG AGTGGCTACA CTTTCTGAGC 180
CTCGGCTTTC TTGGCTGTTA AATTGATATG TATATACAAG CGCCCTCTGC ATAGCAGGGC 240
TTCTCAGACC CAACACTATT GACATTTTGG GCTGGATAAT TCTTTGTTGT GAGGCTGTCC 300
TGTGCATTGC AGGATGTTTA GCGGTATCCC TGGCCTCTAC CACATAGGGT ATTCACTGCC 360
AAGAGATGCC AGTAGCAACT CCCACTCAAG CTGTGACAAA CCTAAAATGT CCCCTGATCT 420
TGCCAAATGT CCTCTGGGGG CAAAATCAAC CCTAGTTTAG AACCACTGCC TAATAGGATC 480
CTGGGGAGGA TTAAATGAGC TATTTCATAT AAAATACCTT CCGGCAATCC CTTCCCCATT 540
CCTTCCATAA CTCTATGGTG AGTTCTAACT CCTCAGAACC CTCTTGTTCT TTCTGTTCCT 600
CTACTGTTTG GAAAATGTGC CCACCTATGG AGACTGGGTG CTTGAGAGCT TCTTGCAAAT 660
CCAAAGCTGT TCCAGGAGCT AGACCTGATT CCAGTCCTGT CATTTCCACA GACATGCTGT 720
GGGACCTTGG CTGAAGTCCT TCCCCTCCTT GAGCCTCGGT TTCCCCATGT GTACGAGGGG 780
GCTGACCCAG AAGCTTTCCG AAAGGTCTTC TCACTGCAGG AATCAGTGAC TGGGTGATTC 840
ATACCAAGTG CAAATTCCCC TCACAAAGTC CAAATTCTTC CAGCGACTTA GTCATTCCAG 900
GGTTTGAACT TTCTCGCAAA AACCATTTGA AAAATTCTTC CAGCTTAAAA AAAAAAAAAA 960
AAAGCTATTA AAAGAAAGTA AAAGTTTCAA AACCAAATCC TAGGCAAACA ACCCTGAAAA 1020
CAATACACAC ACATACATAT ACATACAGCA CCCAAGGTAG CTCTGAGAAC AGGATATGAA 1080
ACCTTGCAGG CCGGCACTAA GAAATGATTC ACAGGCCTTT GAGATGCTTC TATTTCAAGA 1140
CACAGTCCAC CCACTGGATC TGGTGGCTCC AAAAACAAAC TTTCAGCTGC TGTTTCTTAT 1200
CGCAGTGTGG TTCGCCTGGC CAGTATCCTT GGGTCTCAAG AGCTCCAGAC AGAAGACAAG 1260
GTTGAGTCCT GTGAATTCCC TTTCTGTTCT ATTTCAAGCC TCAAGCTGCT GGCTTGTTTA 1320
AAGAAAGTCT TTTGCATCCA CCTTTTGGTT GGCTGACCCG AGTTTAAAGC AACATAGCCT 1380
AATGGGTTCG TAGCACAGCC TGCGAATTCA TAATTTTAGT TTAGCAAGGC CTCTGTGTGG 1440
CTCCAGCAAG TCCTACTGGA TCCTGGGCTG GTCATTCTAG AAGCTGTCTC CAGCTAAACA 1500
ATCCTGCCTG GCTTTCCTTA TACATATCAA TATTATACTT GCCCTAGGCC AGGATTAAGA 1560
ATTTTAGCAC AAATTCAAAA TTTCATGCTT TTATGTAAAA TAGAAATATA AAAGTAATTC 1620
ATTCGATGAA ATGCTTACTG AGTGCTCACT ATATGCCAAG CACCAGCAAT GTACTGGCGA 1680
TAAAATACAG CCCCTGCCTT CAGGAGCCAC ATTGAACAGG 1720