Variant report

Variant	rs806977
Chromosome Location	chr6:26189615-26189616
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:152)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:152 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TEAD4	chr6:26188981-26189679	SK-N-SH	brain:	n/a	n/a
2	CEBPD	chr6:26188043-26189749	K562	blood:	n/a	n/a
3	SIN3AK20	chr6:26188361-26189692	K562	blood:	n/a	n/a
4	POLR2A	chr6:26186579-26189799	H1-hESC	embryonic stem cell:	n/a	n/a
5	ZBTB33	chr6:26188018-26189693	SK-N-SH	brain:	n/a	n/a
6	POLR2A	chr6:26187922-26189658	PANC-1	pancreas:	n/a	n/a
7	MYBL2	chr6:26188167-26189684	HepG2	liver:	n/a	n/a
8	POLR2A	chr6:26188194-26189635	ProgFib	skin:	n/a	n/a
9	PML	chr6:26188071-26189691	GM12878	blood:	n/a	n/a
10	POLR2A	chr6:26188120-26190099	K562	blood:	n/a	n/a
11	CREB1	chr6:26188406-26189685	GM12878	blood:	n/a	n/a
12	POLR2A	chr6:26187684-26208312	K562	blood:	n/a	n/a
13	TRIM28	chr6:26188088-26189734	K562	blood:	n/a	n/a
14	CEBPB	chr6:26188134-26189685	HCT-116	colon:	n/a	n/a
15	JUND	chr6:26188956-26189695	SK-N-SH	brain:	n/a	n/a
16	RXRA	chr6:26189146-26189625	GM12878	blood:	n/a	n/a
17	PML	chr6:26188456-26189686	MCF-7	breast:	n/a	n/a
18	NFIC	chr6:26188340-26189680	HepG2	liver:	n/a	n/a
19	EP300	chr6:26188605-26189670	A549	lung:	n/a	n/a
20	TCF12	chr6:26188046-26189769	SK-N-SH	brain:	n/a	n/a
21	MXI1	chr6:26188478-26189634	GM12878	blood:	n/a	n/a
22	ZBTB33	chr6:26188161-26189646	A549	lung:	n/a	n/a
23	PBX3	chr6:26188926-26189644	SK-N-SH	brain:	n/a	n/a
24	BCLAF1	chr6:26188187-26189619	GM12878	blood:	n/a	n/a
25	POLR2A	chr6:26187993-26189618	H1-hESC	embryonic stem cell:	n/a	n/a
26	FOXM1	chr6:26188203-26189705	GM12878	blood:	n/a	n/a
27	SP1	chr6:26188513-26189733	A549	lung:	n/a	chr6:26189278-26189289
28	JUND	chr6:26188189-26189698	HCT-116	colon:	n/a	n/a
29	MAX	chr6:26188199-26189673	A549	lung:	n/a	chr6:26188885-26188892 chr6:26188884-26188893
30	SP4	chr6:26188073-26189682	H1-hESC	embryonic stem cell:	n/a	chr6:26189278-26189289
31	TEAD4	chr6:26188114-26189668	K562	blood:	n/a	n/a
32	CBX3	chr6:26188120-26189722	HCT-116	colon:	n/a	n/a
33	MAX	chr6:26188292-26189673	HepG2	liver:	n/a	chr6:26188885-26188892 chr6:26188884-26188893
34	ZEB1	chr6:26188338-26189697	HepG2	liver:	n/a	n/a
35	MAX	chr6:26188117-26189681	A549	lung:	n/a	chr6:26188885-26188892 chr6:26188884-26188893
36	SP1	chr6:26188374-26189725	HCT-116	colon:	n/a	chr6:26189278-26189289
37	ATF2	chr6:26188535-26189659	GM12878	blood:	n/a	n/a
38	HDAC2	chr6:26189044-26189641	MCF-7	breast:	n/a	n/a
39	POLR2A	chr6:26188030-26189654	GM12878	blood:	n/a	n/a
40	FOXM1	chr6:26188377-26189643	SK-N-SH	brain:	n/a	n/a
41	ELF1	chr6:26188787-26189678	SK-N-SH	brain:	n/a	n/a
42	SP1	chr6:26189043-26189616	HepG2	liver:	n/a	chr6:26189278-26189289
43	MAX	chr6:26189101-26189635	SK-N-SH	brain:	n/a	n/a
44	ATF2	chr6:26187935-26189633	H1-hESC	embryonic stem cell:	n/a	n/a
45	MBD4	chr6:26188119-26189620	HepG2	liver:	n/a	n/a
46	POLR2A	chr6:26188149-26189643	U87	brain:	n/a	n/a
47	PBX3	chr6:26189053-26189639	SK-N-SH	brain:	n/a	n/a
48	POLR2A	chr6:26188088-26189669	H1-neurons	neurons:	n/a	n/a
49	FOXM1	chr6:26188175-26189643	GM12878	blood:	n/a	n/a
50	TEAD4	chr6:26188160-26189625	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26189597-26189647	HEK293	kidney:	embryo
2	chr6:26189597-26189647	NHDF-neo	bronchial:	n/a
3	chr6:26189597-26189647	HepG2	liver:	n/a
4	chr6:26189597-26189647	ECC-1	luminal epithelium:	n/a
5	chr6:26189597-26189647	BE2_C	brain:	n/a
6	chr6:26189597-26189647	SK-N-MC	brain:	n/a
7	chr6:26189597-26189647	Hela-S3	cervix:	n/a
8	chr6:26189597-26189647	HRCEpiC	kidney:	n/a
9	chr6:26189597-26189647	NB4	blood:	n/a
10	chr6:26189597-26189647	HCPEpiC	choroid plexus:	n/a
11	chr6:26189597-26189647	BJ	skin:	n/a
12	chr6:26189597-26189647	HCT-116	colon:	n/a
13	chr6:26189597-26189647	HL-60	blood:	n/a
14	chr6:26189597-26189647	NHBE	bronchial:	n/a
15	chr6:26189597-26189647	IMR90	lung:	fetal
16	chr6:26189597-26189647	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:26189597-26189647	GM12878	blood:	n/a
18	chr6:26189597-26189647	NH-A	brain:	n/a
19	chr6:26189597-26189647	SKMC	muscle:	n/a
20	chr6:26189597-26189647	MCF-7	breast:	n/a
21	chr6:26189597-26189647	GM19239	blood:	n/a
22	chr6:26189597-26189647	HRPEpiC	eye:	n/a
23	chr6:26189597-26189647	PANC-1	pancreas:	n/a
24	chr6:26189597-26189647	Jurkat	blood:	n/a
25	chr6:26189597-26189647	AG09319	gingival:	n/a
26	chr6:26189597-26189647	HAEpiC	amniotic membrane:	n/a
27	chr6:26189597-26189647	H1-hESC	embryonic stem cell:	embryo
28	chr6:26189597-26189647	PFSK-1	brain:	n/a
29	chr6:26189597-26189647	MCF10A-Er-Src	breast:	n/a
30	chr6:26189597-26189647	HIPEpiC	eye:	n/a
31	chr6:26189597-26189647	HEEpiC	esophagus:	n/a
32	chr6:26189597-26189647	AG04450	lung:	fetal
33	chr6:26189597-26189647	T-47D	breast:	n/a
34	chr6:26189597-26189647	HUVEC	blood vessel:	n/a
35	chr6:26189597-26189647	RPTEC	kidney:	n/a
36	chr6:26189597-26189647	LNCaP	prostate:	n/a
37	chr6:26189597-26189647	SK-N-SH	brain:	n/a
38	chr6:26189597-26189647	NT2-D1	testis:	n/a
39	chr6:26189597-26189647	AG10803	skin:	n/a
40	chr6:26189597-26189647	ovcar-3	ovarian:	n/a
41	chr6:26189597-26189647	HRE	kidney:	n/a
42	chr6:26189597-26189647	HMEC	breast:	n/a
43	chr6:26189597-26189647	AoSMC	blood vessel:	n/a
44	chr6:26189597-26189647	HCF	heart:	n/a
45	chr6:26189597-26189647	A549	lung:	n/a
46	chr6:26189597-26189647	SK-N-SH_RA	brain:	n/a
47	chr6:26189597-26189647	CMK	blood:	n/a
48	chr6:26189597-26189647	GM12892	blood:	n/a
49	chr6:26189597-26189647	ProgFib	skin:	n/a
50	chr6:26189597-26189647	SAEC	small airway:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26187375..26189880-chr6:27097420..27103446,8	K562	blood:
2	chr6:26026488..26028214-chr6:26187877..26190582,2	MCF-7	breast:
3	chr6:26188276..26190980-chr6:26381179..26383865,2	K562	blood:
4	chr6:26187831..26190328-chr6:26520761..26523308,3	K562	blood:
5	chr20:45985042..45987861-chr6:26187518..26190404,2	MCF-7	breast:
6	chr5:180659417..180661225-chr6:26188646..26190614,2	K562	blood:
7	chr6:26188869..26191553-chr6:26538652..26541093,2	K562	blood:
8	chr6:26187687..26190163-chr6:27098059..27101507,5	K562	blood:
9	chr6:26187662..26190884-chr6:27112568..27116666,4	MCF-7	breast:
10	chr12:122150220..122151057-chr6:26188979..26189750,2	NB4	blood:
11	chr6:26054932..26056773-chr6:26188728..26190968,2	MCF-7	breast:
12	chr1:25573445..25574165-chr6:26188934..26189726,2	NB4	blood:
13	chr6:26187257..26192079-chr6:27098954..27103250,7	MCF-7	breast:
14	chr6:26187760..26190799-chr6:26518890..26523308,5	K562	blood:
15	chr6:26187507..26190261-chr6:27099153..27102365,6	MCF-7	breast:
16	chr17:7387332..7388065-chr6:26189234..26189746,2	NB4	blood:

No data

Variant related genes	Relation type
HIST1H4D	TF binding region
HIST1H4D	CpG island
ENSG00000146063	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000188735	Chromatin interaction
ENSG00000199289	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000181222	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000228223	Chromatin interaction
ENSG00000124529	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000174282	Chromatin interaction
ENSG00000124508	Chromatin interaction
ENSG00000182952	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000117616	Chromatin interaction
ENSG00000187837	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1059486	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1543681	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2179517	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2393592	0.81[GIH][hapmap]
rs3999544	0.81[GIH][hapmap];0.83[MEX][hapmap]
rs4145878	0.89[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap]
rs6935954	0.88[CHB][hapmap];0.86[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.80[TSI][hapmap]
rs806789	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs806795	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.87[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs806798	0.81[EUR][1000 genomes]
rs9393692	0.81[GIH][hapmap];0.87[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
8	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
9	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
10	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
11	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
12	nsv1025493	chr6:26026870-26223838	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1001 gene(s)	inside rSNPs	diseases
13	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
14	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
15	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
16	nsv482348	chr6:26082709-26261136	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	799 gene(s)	inside rSNPs	diseases
17	nsv518431	chr6:26148311-26211368	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases
18	nsv526456	chr6:26148311-26211368	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases
19	nsv883490	chr6:26172219-26231608	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	316 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs806977	PRSS16	cis	parietal	SCAN
rs806977	HIST1H2AH	cis	cerebellum	SCAN
rs806977	BTN3A2	cis	lymphoblastoid	seeQTL
rs806977	ZSCAN23	cis	cerebellum	SCAN
rs806977	HIST1H4F	cis	parietal	SCAN
rs806977	LRRC16A	cis	parietal	SCAN
rs806977	HIST1H3E	cis	cerebellum	SCAN
rs806977	HIST1H2AK	cis	parietal	SCAN

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26182000-26193000	Weak transcription	Dnd41	blood
2	chr6:26188000-26189800	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr6:26188000-26189800	Active TSS	Fetal Brain Female	brain
4	chr6:26188000-26189800	Active TSS	Fetal Kidney	kidney
5	chr6:26188200-26189800	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr6:26188200-26189800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr6:26188200-26190000	Active TSS	Rectal Smooth Muscle	rectum
8	chr6:26188400-26189800	Active TSS	Aorta	Aorta
9	chr6:26188800-26189800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
10	chr6:26188800-26190000	Active TSS	Brain Germinal Matrix	brain
11	chr6:26188800-26190000	Active TSS	GM12878-XiMat	blood
12	chr6:26188800-26190200	Active TSS	Colon Smooth Muscle	Colon
13	chr6:26189000-26190000	Active TSS	K562	blood
14	chr6:26189200-26189800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:26189200-26189800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
16	chr6:26189200-26189800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:26189200-26190200	Active TSS	Rectal Mucosa Donor 29	rectum
18	chr6:26189200-26190400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr6:26189200-26190400	Enhancers	Fetal Heart	heart
20	chr6:26189400-26189800	Flanking Active TSS	Primary B cells from cord blood	blood
21	chr6:26189400-26189800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr6:26189400-26189800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:26189400-26189800	Enhancers	Fetal Brain Male	brain
24	chr6:26189400-26189800	Active TSS	Psoas Muscle	Psoas
25	chr6:26189400-26190000	Enhancers	Liver	Liver
26	chr6:26189400-26190200	Enhancers	Primary B cells from peripheral blood	blood
27	chr6:26189400-26190200	Enhancers	Primary T cells fromperipheralblood	blood
28	chr6:26189400-26190200	Active TSS	Stomach Smooth Muscle	stomach
29	chr6:26189400-26190400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr6:26189400-26190400	Enhancers	Duodenum Mucosa	Duodenum
31	chr6:26189400-26190600	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr6:26189400-26193800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:26189400-26193800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr6:26189400-26193800	Weak transcription	Hela-S3	cervix
35	chr6:26189400-26194600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr6:26189400-26195000	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr6:26189400-26195200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr6:26189400-26195200	Weak transcription	NHLF	lung
39	chr6:26189400-26195400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr6:26189400-26195400	Weak transcription	HMEC	breast
41	chr6:26189400-26195800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr6:26189600-26189800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr6:26189600-26189800	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr6:26189600-26189800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr6:26189600-26189800	Flanking Active TSS	Thymus	Thymus
46	chr6:26189600-26189800	Weak transcription	A549	lung
47	chr6:26189600-26189800	Enhancers	NHEK	skin
48	chr6:26189600-26190000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr6:26189600-26190000	Enhancers	Fetal Muscle Trunk	muscle
50	chr6:26189600-26190000	Enhancers	Placenta	Placenta

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