EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS002-00332 
Organism
Homo sapiens 
Tissue/cell
A375 
Coordinate
chr1:43406710-43408630 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6657798chr143408279hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr1:43406837-43406851CTGAGTCATTTCCC-6.06
NFE2L1MA0089.2chr1:43407593-43407608GCATGACTCAGCAGG+6.75
Nfe2l2MA0150.2chr1:43407591-43407606GAGCATGACTCAGCA+7.66
ZNF263MA0528.1chr1:43407030-43407051CCCCAACCTTTCCCCTCCTCC-6.09
ZNF263MA0528.1chr1:43408088-43408109CCTTTTCCTCTTCTCTCCTCC-6
Number of super-enhancer constituents: 50             
IDCoordinateTissue/cell
SE_01795chr1:43403674-43411142Aorta
SE_02447chr1:43405569-43410613Astrocytes
SE_04284chr1:43406405-43408666Brain_Anterior_Caudate
SE_05390chr1:43406422-43410832Brain_Cingulate_Gyrus
SE_06192chr1:43406287-43411226Brain_Hippocampus_Middle
SE_07319chr1:43406534-43411143Brain_Hippocampus_Middle_150
SE_08269chr1:43406272-43411134Brain_Inferior_Temporal_Lobe
SE_10377chr1:43406726-43412417CD19_Primary
SE_11009chr1:43387831-43425728CD20
SE_13825chr1:43406488-43407528CD34_Primary_RO01536
SE_14471chr1:43395753-43414527CD4_Memory_Primary_7pool
SE_19657chr1:43406292-43410967CD4p_CD25-_Il17p_PMAstim_Th17
SE_20345chr1:43407577-43412424CD56
SE_20799chr1:43405756-43409955CD8_Memory_7pool
SE_22754chr1:43406075-43412634CD8_primiary
SE_23189chr1:43406366-43410995Colon_Crypt_1
SE_23904chr1:43406747-43407203Colon_Crypt_2
SE_23904chr1:43407223-43410890Colon_Crypt_2
SE_25177chr1:43406652-43411022Colon_Crypt_3
SE_26580chr1:43395721-43413249Esophagus
SE_29267chr1:43400819-43410293Fetal_Intestine_Large
SE_31882chr1:43406451-43411068Gastric
SE_33837chr1:43401475-43412846HCC1954
SE_34353chr1:43395339-43412997HCT-116
SE_35049chr1:43400682-43411164HeLa
SE_36013chr1:43405529-43411011HMEC
SE_37191chr1:43404622-43414101HSMMtube
SE_38794chr1:43405440-43410875HUVEC
SE_39883chr1:43405665-43410931K562
SE_41038chr1:43405665-43414583Left_Ventricle
SE_41620chr1:43406373-43411014LNCaP
SE_42796chr1:43405575-43411121Lung
SE_49782chr1:43406287-43407314Right_Ventricle
SE_49782chr1:43407568-43410944Right_Ventricle
SE_50202chr1:43406339-43411463Sigmoid_Colon
SE_54088chr1:43406450-43408242Spleen
SE_55340chr1:43407386-43410138Thymus
SE_55821chr1:43405505-43410178u87
SE_57045chr1:43406294-43410932VACO_400
SE_57417chr1:43405825-43410963VACO_503
SE_58269chr1:43406518-43407187VACO_9m
SE_58269chr1:43407361-43407923VACO_9m
SE_58269chr1:43408012-43408449VACO_9m
SE_58561chr1:43388242-43430420Ly1
SE_60624chr1:43388552-43428820DHL6
SE_62392chr1:43388423-43425814Tonsil
SE_64094chr1:43405747-43410036HSMM
SE_64340chr1:43405657-43411071NHEK
SE_67781chr1:43405505-43410178u87
SE_68708chr1:43406265-43410984H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14340735543407700
Number: 1             
IDChromosomeStartEnd
GH01I042929chr14339554143414526
Enhancer Sequence
GATGACCAAA TCCTGTCCAT TCTTCCTCTG AGGGTTTGCT TTTATGTCAC TAGTCCAACG 60
GCAACTTTCT TGATGGTTTC CCGTCTCTAG TCTCACATTC TTAAGTCCGC CCCTCCATAC 120
CAGACGCCTG AGTCATTTCC CTACAATGCA AGTCTGATCA CGTCTGCCCT GGGCAGTGGG 180
TCCCTATTGT CCTCATCCTG AAGTCCATGC TCCCTAGCTG GGCCCCCGTG CTGGTGCCCA 240
TCCGCCCCTT CTGACTGTGC CGTGCCATAC TCACAAGGCC CTTTGTGGTC TGGCTCTTGC 300
CTACCTTACC TTGTTGACCT CCCCAACCTT TCCCCTCCTC CTGTTCACTC TAGTGACACA 360
CTAAACTACT CACGCTTTAC TGAATGCCAG GCTTTCTGTC TTCTGGGCAT TTTGCTTTGA 420
AGGCCCCCTG CTCACCCCAA CCCTGTTCTG TTTCTGGAAA ACACCTCCTC TGTCCTGGCC 480
TTAGAGTCCT AGTTCTGTCA TTAACTCACT ATGAGATCAC AGTCAAGACA TCATTAAATC 540
CAGTAGCTGT CAACCTTGGC TGCACATTCG AATTGGTTGG GAAGCTTTTA ATTGAATGCC 600
CAAACAGCAT CCCAGACCAA TTAAATCAGA ATCTGGGGGC GTTCTGGAAA CCCCAATGTG 660
CAACCAAGTG GAGAGCTCAA CCTCCCTCTG TTTCCTCCCA GCCTGTCTTA CAGACTTTCC 720
ATCTGTAAGG ATTCCCAAAG GGAGCCAGTT CTGAAGCACA CACTTTGGCA AGAGCTGTCA 780
AGAGCACTTA GCAAATGCAG GGCTTGGGGC TGGTCCAAGC ATGGGCCCAC GGTCTCCATG 840
CCCAGCAAAC TTGGAAAAGT CCTGTCACCT CCCCTGCAGC TGAGCATGAC TCAGCAGGCC 900
AAGCCTTCCT GGTGACTTGC TCCTCAGCAT CGGGCGTGGC CCCATAGCCA CTGTCTGCCT 960
ATTTGGAAGA AGCCCAGCTA ACTCTAGACA CTACCTGGTT CCCCCAAACA GGACCCTGAT 1020
CTTTGGGAGT CACTGCACTC ACTTTCTAGC CCCATCCGTC TGGACAAGAA ATGTGGTCCT 1080
GACGTGAGGA CTGCCCACTC TCATTTGGTC CTCTCTGGGA AGGTACAGAT TTTTAAACGG 1140
GCAAGGCAGC TGGTTAGGAA GACAACCTGA GGCCATGGAA ACAACAGAGC TTGGCTTCTG 1200
ACTCCAGCAT TCAATAGCTT TGTGACCTTG GGCCTGTCGG CCATTTCATC TGCCTGGGCC 1260
TCAGTTTCCG GGTCTACAAA ATGGAAATCA CCACCCAATC TCATAAACAC AAGCAAAATG 1320
CCTGGTACAG AGGAAGGGCT CAGTTTCCTT TCCTGTCCCT GCCTCCTACC CCCTACCCCC 1380
TTTTCCTCTT CTCTCCTCCT TAATGCAAGT AGGCTGGGCT GGAGGAGATG GTCTAGGTCC 1440
CTTCCCATCC TGACATTCAA GTAAACAAGT GAGGACAGAT CTAGGATGCA CGGCAGGGAG 1500
GAGGAAGCCA GCACAGACCT TCACCCCCTG TGGCTCCCTA GGGCAAGACG CCATTTCTGC 1560
TTTGACTGCC ACAGGGCCTT CAGGGAGAGG ACGCGGTTTC AACCTACAAA TAAAGGAAGT 1620
GTGCTGCCTG TGGATGGGTA TGAGTGCAGG CTCAAGGACC ACCTGGCAGG CAGGTGTTGG 1680
ATACCAGCTC TGTCTCTGAC TTAGCTGGGT GATATTGGGC GGGTTTCCTC TCTCTGGCCG 1740
TTTCCCACAC CTGCAGGCTG GGAGTGGTGC CTGCTGCCTC CTGACAGTGC TGCAGTGAGC 1800
ATCAAGTGAG ACAAGCCCAT GAAAACCCTC TGCAGCCCCA GAATGCCACG GAAATGCAGC 1860
ATTATTGTAT TGAGCTTTGC TTTGAGTTTA TTATATCATC AAACATATTA TTAAATGACT 1920