EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS176-25170 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr22:36778460-36779840 
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_01541chr22:36778883-36779796Aorta
SE_09195chr22:36778886-36780059CD14
SE_10697chr22:36778920-36779883CD19_Primary
SE_11020chr22:36744527-36785336CD20
SE_11868chr22:36778822-36779919CD3
SE_13866chr22:36778868-36779843CD34_Primary_RO01536
SE_15488chr22:36779024-36780057CD4_Memory_Primary_8pool
SE_16465chr22:36778877-36779982CD4_Naive_Primary_8pool
SE_16932chr22:36779031-36779804CD4p_CD225int_CD127p_Tmem
SE_17339chr22:36756664-36780212CD4p_CD25-_CD45RAp_Naive
SE_17788chr22:36746596-36785463CD4p_CD25-_CD45ROp_Memory
SE_18286chr22:36778872-36780104CD4p_CD25-_Il17-_PMAstim_Th
SE_19119chr22:36778850-36779887CD4p_CD25-_Il17p_PMAstim_Th17
SE_20220chr22:36778822-36779857CD56
SE_21488chr22:36778906-36780027CD8_Naive_7pool
SE_21957chr22:36778770-36780051CD8_Naive_8pool
SE_22328chr22:36778854-36780054CD8_primiary
SE_23071chr22:36779245-36779728Colon_Crypt_1
SE_23740chr22:36779319-36779741Colon_Crypt_2
SE_26521chr22:36778719-36784910Esophagus
SE_30956chr22:36779016-36779820Fetal_Thymus
SE_31378chr22:36778887-36780652Gastric
SE_40597chr22:36778965-36779811Left_Ventricle
SE_41574chr22:36779208-36779810LNCaP
SE_42094chr22:36778767-36779937Lung
SE_45604chr22:36778918-36779846Osteoblasts
SE_47463chr22:36779022-36779672Pancreas
SE_50050chr22:36778697-36779840Sigmoid_Colon
SE_52340chr22:36778771-36779932Small_Intestine
SE_53283chr22:36778868-36780625Spleen
SE_54489chr22:36779015-36780052Stomach_Smooth_Muscle
SE_55183chr22:36778929-36779740Thymus
SE_58448chr22:36724049-36832686Ly1
SE_62151chr22:36773097-36852649Toledo
SE_62244chr22:36719186-36785326Tonsil
SE_67374chr22:36778698-36784244MM1S
SE_68689chr22:36779135-36779745H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr223677888336779721
Enhancer Sequence
AGTGAGCCGA GATCACACCA CTGCACTCCA GCCTGGGCAA CAGAGCGAGA CTCAGTCTCA 60
AAAAACAAAA AAAAGAGTGC CTAGGAAATT AAAATTACTT GATTTTGCTG GGTGTGGTGG 120
CTCATGCCTA TAATCCCAGC ACTTTGGGAG GCCAAGGCGG GTGGATCGCC TGAGGTCGGA 180
AGTTCGAGAC CAGCCTGGCC AACGTGGTGA AACCCCATCT CTACTAAAAA TGCAAAAACT 240
AGCCGGGTGT GGTGGTGCAC CCCTGTAATC CTGGCTACTC GGTAGGCTGA GGTAGGAATA 300
TTGCTTGAAC CCAGGAGGCA GAGGCTGCAG TGAGCCAAGA TCATGCCACT GTACTCCAGC 360
CTGGGCAACA GAGTGAGACC CCATCTCAAA TAAAGAAATA AATAAATAAA TAAAATTACT 420
TAATTTTTCA GTTTTTCAGG CACTCCCATA CATAACTTGT GGGCACATAA ACTGGTATGA 480
TATCTTTGTA GGGAGATACG GCACCTCCTC GGAAATCAAA CCTGGCCAGG TGCAGTATTT 540
CACACCTGTA ACCCCAGCAC TCTGAGAGGC TGAGGCAGGA GGGTTGCTTG AGCCCAGGGG 600
TTTGAGACTA GCCTAGGCAA TACAGCAAGA TCCCATCCCT ACAAAAAACA CAAAAATTAG 660
CCAGGTGTAG CAGTGTGCAC TTGTAATCCT GGCTACTCAG GAGGCTGAGG CAGAGAATTG 720
CTTGAGCCCA GGAATTTGAG GCTGCAGTGA GCTATGATCA TGCTACTGCA CTATAGCCTG 780
GGCAACAGAG CAAGACCCTG CTTCAAAACG AAATCAAAAA ACAAAAAGGA AATCAAACCT 840
CCCCTCACCC AGAGCCAGAG TTGGAAGTAA GGTCTCCAGT CACCCAAGTC CAGTGCTCTT 900
CCTGTATCAC CCTTTGGCTA TCTCCCAGAC CACAGGAAAC CATGTGTTTG AACTGAAACC 960
ACAGTCTGCA CACCTTCTGT CCCAGCCGGG GCCCTGTGAA GAGGTTACTC AGCAGAAGTT 1020
CATCACCAAG TGCATCCAAA AGCATCAGCA GATGGGCCTC ATAGCCACTT GTGAATAGGC 1080
AGTCCACAAC CACAGTCCAC AACCACAATA CACGCATACC TTGTTGTGCA CAGAGGCAGA 1140
AAGAACACCG AGCTAGAAGC CAGGAAAACA ATCTGTCCCC CAGCCTCATC CCCACCCCCT 1200
CAACCTGATA ACCTAGGGAG TTAAGACTGA TCATTTATAT TAAAAAAAAA GGGGGGGGGG 1260
TGCCAGGTGC GGTGGCTCAC GCCTGTAATC CTAACACTTT GGGAGGCTGA GGCGGGTAGA 1320
TCACCTGAGG TCAGGAGCTC GAGACCAGCC TGGCCAACAT AGTGAAACCC TGTCTCTACT 1380