EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS176-20560 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr2:54799330-54800580 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10205410chr254799599hg19
Number of super-enhancer constituents: 58             
IDCoordinateTissue/cell
SE_00006chr2:54795695-54808079Adipose_Nuclei
SE_00896chr2:54799791-54802361Adrenal_Gland
SE_02562chr2:54796678-54802057Astrocytes
SE_04102chr2:54799690-54802108Brain_Anterior_Caudate
SE_10400chr2:54794677-54803227CD19_Primary
SE_11005chr2:54790737-54825699CD20
SE_11903chr2:54795467-54804954CD3
SE_12885chr2:54798660-54800004CD34_Primary_RO01480
SE_13387chr2:54797492-54801918CD34_Primary_RO01536
SE_14098chr2:54798186-54800123CD34_Primary_RO01549
SE_14488chr2:54795303-54804872CD4_Memory_Primary_7pool
SE_15498chr2:54795663-54803273CD4_Memory_Primary_8pool
SE_15859chr2:54798421-54804026CD4_Naive_Primary_7pool
SE_16386chr2:54795629-54803366CD4_Naive_Primary_8pool
SE_16936chr2:54795657-54803270CD4p_CD225int_CD127p_Tmem
SE_17333chr2:54793892-54821363CD4p_CD25-_CD45RAp_Naive
SE_17873chr2:54795021-54811216CD4p_CD25-_CD45ROp_Memory
SE_18341chr2:54795035-54821330CD4p_CD25-_Il17-_PMAstim_Th
SE_19520chr2:54795631-54804015CD4p_CD25-_Il17p_PMAstim_Th17
SE_20164chr2:54795681-54809753CD56
SE_20822chr2:54795629-54803439CD8_Memory_7pool
SE_21502chr2:54795741-54803316CD8_Naive_7pool
SE_21966chr2:54795626-54804551CD8_Naive_8pool
SE_22380chr2:54795196-54811289CD8_primiary
SE_23128chr2:54797995-54802474Colon_Crypt_1
SE_23914chr2:54799575-54801320Colon_Crypt_2
SE_25070chr2:54797970-54802593Colon_Crypt_3
SE_25877chr2:54795570-54803197Duodenum_Smooth_Muscle
SE_27348chr2:54798913-54803836Esophagus
SE_27627chr2:54794756-54809409Fetal_Intestine
SE_28537chr2:54794775-54810703Fetal_Intestine_Large
SE_29772chr2:54797867-54801835Fetal_Muscle
SE_31160chr2:54795567-54803312Fetal_Thymus
SE_31545chr2:54798932-54799520Gastric
SE_31545chr2:54799542-54802418Gastric
SE_32493chr2:54794685-54809919GM12878
SE_35301chr2:54797810-54803653HeLa
SE_35875chr2:54796741-54804603HMEC
SE_38000chr2:54795734-54802579HUVEC
SE_39396chr2:54795484-54802646Jurkat
SE_40773chr2:54796706-54802488Left_Ventricle
SE_42137chr2:54796708-54803360Lung
SE_43945chr2:54794597-54799592MM1S
SE_46220chr2:54795768-54803253Osteoblasts
SE_47832chr2:54799847-54801132Pancreas
SE_49907chr2:54795402-54803294RPMI-8402
SE_50115chr2:54795848-54803359Sigmoid_Colon
SE_52386chr2:54795955-54803388Small_Intestine
SE_53342chr2:54795939-54803322Spleen
SE_55277chr2:54799481-54802818Thymus
SE_56813chr2:54799680-54801306VACO_400
SE_57612chr2:54799687-54800303VACO_503
SE_60008chr2:54784446-54818579Ly4
SE_61167chr2:54784367-54847020HBL1
SE_61474chr2:54749764-54818736Toledo
SE_62304chr2:54783676-54846716Tonsil
SE_64270chr2:54795687-54804439NHEK
SE_66257chr2:54795484-54802646Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr25480004554800558
Number: 1             
IDChromosomeStartEnd
GH02I054566chr25479411254810964
Enhancer Sequence
AGACATCACA TTGTCTTTTT CCCCCCTTTC TTTTGAATGA GATGGGGCAA GAATATTTGG 60
ACCAGGATAA AGTTTTAAGA TGCATTTACA CTAATGTAAT CAGGTTACAT AGCAAAAAAA 120
TGTTAAAAAT GTACCCTGGG AAATTGAAAT CTATCCATTC TTCTAGGTGT GGCAGCTTAT 180
TCAGATTTTT ATGTTGTGTG ACCATAAAAC GAACACAGCT TTTCTAACCG CGAGTGTCTT 240
TGTTTACAGA GATAACAGTG TGAGTAATGC TTTGCTAGAA GCCAGGCAGT TAAATCACAC 300
TCTGAGCAAA TAGAGGCTGG GCTTCAGAAA CTTAGATAGC ACACGAATGT GCAAACTTGG 360
TCTTTTAAAC TGAAGACATA TCTGAAAGAA AACTGCTTTT GGCCCATGAA CTACTTTCCC 420
AGCCCTTTGT GCCTCCCAAT CTCTGCCCCC CTTTACAAAA AATCTTTGTT TTTCCTCTAC 480
AAATATACAT ATATGATTTC AATTTGGAGG TGGGATGTTA TTTTTTTCAC TTGAAACACA 540
AGGAAGCAAT TTTTAAAAGT CATACTCGTT CAGCAGTGGG CTTGACTGTA GCCAGTTTGA 600
CTAGGAGTTC TTGGCTACAG AACCATACAC TTGCAGTCTT TATCAGGGTA GTAAATTCAG 660
ATGGGTTTTT GGAAAGGGAG AGGGCTGGAG TTGAGGGAAG GGCACTAGAG CAGTGTGACC 720
CACGGCCCAG GAGCAGTGTG AGTGGGAAGG GGCTCTAGAA GCTGACTGCC TTTGTGTTTG 780
CCACAGCGTG CTGGGAATCA GATGAGAAGG CGGGCCCAGA CCCCACCAGA TACTCATCTC 840
AGCCATTGTT GTCATTAAAT GACTCTGAAA TGACCTTTCT TACCTCAGTT TCCTGTGAGC 900
TCATAGTTGT CTGCAGATGT GAATTATGTC ATTGATCTTT GCTCCCTCTT TGCTTATAAG 960
GAGTAGCTGT TCTGCTCCAT GTTTCTGGAA GAGGAAAGTG ATGCACAGGT CACTTAGTAA 1020
AGCGGTCCCC AGCCTTTTTG GCACCAGGGA CTGGTTTTGT AGAAGACAAT TTTTCCACAG 1080
ATAGGGTGGA GGAAATGGGG AGTTGGTTTC GTGATGAAAC TCTTCCACCT CAGATCATCA 1140
GGCATTAGAT TCTTATTAAG GAGTGGTAAC CTAGATCCTT TGCATGCACA GTTCATGATA 1200
GGGTTTGGCT CCTGTGAGAA TGCTGCTGCT GATCTGACAG GAGGCAGAGC 1250