Variant report

Variant	esv3408604
Chromosome Location	chr15:43175709-43207571
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:154)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:154 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:43195629-43195773	K562	blood:	n/a	n/a
2	ARID3A	chr15:43201623-43201823	K562	blood:	n/a	n/a
3	ARID3A	chr15:43203332-43203532	HepG2	liver:	n/a	n/a
4	ATF2	chr15:43182779-43183086	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr15:43200945-43201043	K562	blood:	n/a	n/a
6	BATF	chr15:43196188-43196507	GM12878	blood:	n/a	n/a
7	BATF	chr15:43196217-43196391	GM12878	blood:	n/a	n/a
8	BATF	chr15:43183826-43184145	GM12878	blood:	n/a	chr15:43183946-43183957
9	BATF	chr15:43186195-43186482	GM12878	blood:	n/a	n/a
10	CEBPB	chr15:43203401-43203581	A549	lung:	n/a	chr15:43203404-43203415
11	CEBPB	chr15:43196390-43196412	K562	blood:	n/a	n/a
12	CEBPB	chr15:43203302-43203555	K562	blood:	n/a	chr15:43203404-43203415
13	CEBPB	chr15:43182740-43183284	IMR90	lung:	n/a	n/a
14	CEBPB	chr15:43203284-43203602	Hela-S3	cervix:	n/a	chr15:43203404-43203415
15	CEBPB	chr15:43203303-43203569	HepG2	liver:	n/a	chr15:43203404-43203415
16	CEBPB	chr15:43203248-43203593	IMR90	lung:	n/a	chr15:43203404-43203415
17	CEBPB	chr15:43182737-43183252	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr15:43201598-43201633	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr15:43199000-43199150	GM06990	blood:	n/a	n/a
20	CTCF	chr15:43186120-43186270	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr15:43181857-43181918	Lung_OC	lung:	n/a	n/a
22	CTCF	chr15:43180370-43180400	Lung_OC	lung:	n/a	n/a
23	CTCF	chr15:43188116-43188171	GM20000	blood:	n/a	n/a
24	CTCF	chr15:43199152-43199214	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr15:43199405-43199526	K562	blood:	n/a	n/a
26	CTCF	chr15:43199409-43199488	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr15:43199383-43199548	K562	blood:	n/a	n/a
28	CTCF	chr15:43199108-43199187	GM10248	blood:	n/a	n/a
29	CUX1	chr15:43196341-43196403	K562	blood:	n/a	n/a
30	E2F4	chr15:43176159-43176324	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr15:43183897-43184126	MCF10A-Er-Src	breast:	n/a	n/a
32	EBF1	chr15:43183760-43184251	GM12878	blood:	n/a	n/a
33	EBF1	chr15:43183787-43184145	GM12878	blood:	n/a	n/a
34	EBF1	chr15:43183857-43184174	GM12878	blood:	n/a	n/a
35	EP300	chr15:43182746-43183052	Hela-S3	cervix:	n/a	n/a
36	FOS	chr15:43200778-43201091	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr15:43183847-43184046	MCF10A-Er-Src	breast:	n/a	chr15:43183944-43183955
38	FOS	chr15:43203289-43203584	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr15:43182656-43183086	HUVEC	blood vessel:	n/a	n/a
40	FOS	chr15:43182674-43183150	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr15:43200792-43201116	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr15:43183731-43184183	HUVEC	blood vessel:	n/a	chr15:43183944-43183955
43	FOS	chr15:43182680-43183007	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr15:43182664-43183170	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr15:43183786-43184126	MCF10A-Er-Src	breast:	n/a	chr15:43183944-43183955
46	FOS	chr15:43182578-43183158	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr15:43203313-43203554	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr15:43183909-43184126	MCF10A-Er-Src	breast:	n/a	chr15:43183944-43183955
49	FOS	chr15:43203247-43203597	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr15:43203278-43203586	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43183056-43183106	CMK	blood:	n/a
2	chr15:43183056-43183106	AG09309	skin:	n/a
3	chr15:43183056-43183106	ovcar-3	ovarian:	n/a
4	chr15:43183056-43183106	GM12891	blood:	n/a
5	chr15:43183056-43183106	AoSMC	blood vessel:	n/a
6	chr15:43183056-43183106	IMR90	lung:	fetal
7	chr15:43183056-43183106	PrEC	prostate:	n/a
8	chr15:43183056-43183106	AG09319	gingival:	n/a
9	chr15:43183056-43183106	HRPEpiC	eye:	n/a
10	chr15:43183056-43183106	A549	lung:	n/a
11	chr15:43183056-43183106	AG10803	skin:	n/a
12	chr15:43183056-43183106	GM12878	blood:	n/a
13	chr15:43183056-43183106	ECC-1	luminal epithelium:	n/a
14	chr15:43183056-43183106	SK-N-MC	brain:	n/a
15	chr15:43183056-43183106	SK-N-SH	brain:	n/a
16	chr15:43183056-43183106	HEK293	kidney:	embryo
17	chr15:43183056-43183106	NB4	blood:	n/a
18	chr15:43183056-43183106	HMEC	breast:	n/a
19	chr15:43183056-43183106	MCF10A-Er-Src	breast:	n/a
20	chr15:43183056-43183106	NT2-D1	testis:	n/a
21	chr15:43183056-43183106	K562	blood:	n/a
22	chr15:43183056-43183106	GM19239	blood:	n/a
23	chr15:43183056-43183106	Caco-2	colon:	n/a
24	chr15:43183056-43183106	HCM	heart:	n/a
25	chr15:43183056-43183106	HCT-116	colon:	n/a
26	chr15:43183056-43183106	RPTEC	kidney:	n/a
27	chr15:43183056-43183106	AG04450	lung:	fetal
28	chr15:43183056-43183106	GM06990	blood:	n/a
29	chr15:43183056-43183106	HUVEC	blood vessel:	n/a
30	chr15:43183056-43183106	HAEpiC	amniotic membrane:	n/a
31	chr15:43183056-43183106	SAEC	small airway:	n/a
32	chr15:43183056-43183106	ProgFib	skin:	n/a
33	chr15:43183056-43183106	HRE	kidney:	n/a
34	chr15:43183056-43183106	SK-N-SH_RA	brain:	n/a
35	chr15:43183056-43183106	PANC-1	pancreas:	n/a
36	chr15:43183056-43183106	BJ	skin:	n/a
37	chr15:43183056-43183106	Hela-S3	cervix:	n/a
38	chr15:43183056-43183106	H1-hESC	embryonic stem cell:	embryo
39	chr15:43183056-43183106	BE2_C	brain:	n/a
40	chr15:43183056-43183106	NH-A	brain:	n/a
41	chr15:43183056-43183106	GM12892	blood:	n/a
42	chr15:43183056-43183106	HPAEpiC	pulmonary alveolar:	n/a
43	chr15:43183056-43183106	Hepatocyte	liver:	n/a
44	chr15:43183056-43183106	SKMC	muscle:	n/a
45	chr15:43183056-43183106	HCF	heart:	n/a
46	chr15:43183056-43183106	HL-60	blood:	n/a
47	chr15:43183056-43183106	MCF-7	breast:	n/a
48	chr15:43183056-43183106	PFSK-1	brain:	n/a
49	chr15:43183056-43183106	HRCEpiC	kidney:	n/a
50	chr15:43183056-43183106	HNPCEpiC	eye:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:43201061..43205182-chr15:43207494..43209457,4	K562	blood:
2	chr15:43197523..43199091-chr15:43202841..43204475,2	K562	blood:
3	chr15:43197523..43199091-chr15:43202841..43204475,2	K562	blood:
4	chr15:43169823..43171405-chr15:43172916..43175738,2	K562	blood:
5	chr15:43196236..43198232-chr15:43199329..43201446,2	K562	blood:
6	chr15:43201553..43203286-chr15:43204467..43206953,2	K562	blood:
7	chr15:43194424..43196390-chr15:43210753..43213420,2	K562	blood:
8	chr15:43094398..43098116-chr15:43199741..43201552,3	K562	blood:
9	chr15:43201061..43205182-chr15:43207494..43209457,4	K562	blood:
10	chr15:43204600..43210679-chr15:43210946..43214208,10	K562	blood:
11	chr15:43201553..43203286-chr15:43204467..43206953,2	K562	blood:
12	chr15:43192591..43195469-chr15:43198395..43200582,2	K562	blood:

No data

Variant related genes	Relation type
TTBK2	TF binding region
TTBK2	CpG island
ENSG00000128881	chromatin interactions
ENSG00000260799	chromatin interactions

Extended variants
information (count: 1052 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1052 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192869609	chr15:43175711-43175712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs185338772	chr15:43175725-43175726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577054140	chr15:43175740-43175741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187861998	chr15:43175750-43175751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554721418	chr15:43175754-43175755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541213636	chr15:43175767-43175768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143766227	chr15:43175784-43175785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192913886	chr15:43175796-43175797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569390991	chr15:43175838-43175839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75299236	chr15:43175854-43175855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs76798883	chr15:43175856-43175857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs28392857	chr15:43175949-43175950	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs138879321	chr15:43176041-43176042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532654641	chr15:43176045-43176046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562606382	chr15:43176086-43176087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9806161	chr15:43176088-43176089	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs548430069	chr15:43176121-43176122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149276536	chr15:43176150-43176151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs28613047	chr15:43176165-43176166	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs548945659	chr15:43176183-43176184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570720128	chr15:43176206-43176207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183621980	chr15:43176219-43176220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188260840	chr15:43176235-43176236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569035225	chr15:43176253-43176254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146201866	chr15:43176299-43176300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9806175	chr15:43176320-43176321	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs574894335	chr15:43176323-43176324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181075931	chr15:43176333-43176334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554210193	chr15:43176432-43176433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9806313	chr15:43176466-43176467	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs139100953	chr15:43176512-43176513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547383417	chr15:43176546-43176547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576222969	chr15:43176558-43176559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142301748	chr15:43176563-43176564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555034552	chr15:43176578-43176579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561925222	chr15:43176608-43176609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375373977	chr15:43176632-43176633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs367924580	chr15:43176643-43176644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184834124	chr15:43176732-43176733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576599892	chr15:43176744-43176745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527538377	chr15:43176749-43176750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543939237	chr15:43176770-43176771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547559037	chr15:43176793-43176794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145938839	chr15:43176831-43176832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559488125	chr15:43176842-43176843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552174028	chr15:43176861-43176862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568877043	chr15:43176876-43176877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570421047	chr15:43176928-43176929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537957279	chr15:43176952-43176953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548345032	chr15:43176997-43176998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Autism	19492091	CNVD

Chromatin state (count:373 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43132000-43186800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr15:43136800-43182400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:43142400-43182400	Weak transcription	Lung	lung
4	chr15:43151600-43182400	Weak transcription	Aorta	Aorta
5	chr15:43151800-43178600	Weak transcription	Placenta	Placenta
6	chr15:43154600-43182400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr15:43155000-43182600	Weak transcription	Primary T cells from cord blood	blood
8	chr15:43163400-43176800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr15:43176800-43177000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr15:43177600-43182400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr15:43177800-43185400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr15:43178600-43179200	Enhancers	Placenta	Placenta
13	chr15:43178600-43182600	Weak transcription	Stomach Smooth Muscle	stomach
14	chr15:43179200-43180200	Weak transcription	Placenta	Placenta
15	chr15:43179800-43180000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr15:43179800-43180000	Enhancers	NHEK	skin
17	chr15:43179800-43180200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr15:43180000-43181000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr15:43180200-43181000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr15:43180200-43185600	Enhancers	Placenta	Placenta
21	chr15:43180600-43180800	Enhancers	Psoas Muscle	Psoas
22	chr15:43180600-43180800	Enhancers	Right Ventricle	heart
23	chr15:43180800-43182400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr15:43180800-43182800	Weak transcription	Right Ventricle	heart
25	chr15:43181000-43182400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr15:43181000-43182600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr15:43181000-43182800	Weak transcription	Psoas Muscle	Psoas
28	chr15:43181000-43184000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr15:43181400-43182400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr15:43181600-43182000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr15:43181600-43182400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr15:43181800-43182400	Enhancers	NHEK	skin
33	chr15:43181800-43184400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr15:43181800-43184400	Enhancers	HUVEC	blood vessel
35	chr15:43182000-43182200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr15:43182000-43182400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr15:43182000-43182600	Enhancers	H9 Cell Line	embryonic stem cell
38	chr15:43182000-43184000	Enhancers	HMEC	breast
39	chr15:43182200-43182400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr15:43182200-43182400	Enhancers	NH-A	brain
41	chr15:43182200-43182600	Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr15:43182200-43183200	Enhancers	HSMMtube	muscle
43	chr15:43182200-43184000	Enhancers	Muscle Satellite Cultured Cells	--
44	chr15:43182200-43184400	Enhancers	NHDF-Ad	bronchial
45	chr15:43182400-43182600	Enhancers	Lung	lung
46	chr15:43182400-43182800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr15:43182400-43182800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr15:43182400-43182800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr15:43182400-43182800	Enhancers	Brain Anterior Caudate	brain
50	chr15:43182400-43182800	Flanking Active TSS	NH-A	brain

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